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GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1 AND not provided

Germline classification:
Pathogenic (1 submission)
Last evaluated:
Jun 26, 2018
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of clinical impact:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Somatic classification
of oncogenicity:
None
Review status:
(0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided
Record status:
current
Accession:
RCV000848828.2

Allele description [Variation Report for GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1]

GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1

Genes:
Variant type:
copy number loss
Cytogenetic location:
Xp22.33-q28
Genomic location:
ChrX: 168546 - 155233731 (on Assembly GRCh37)
Preferred name:
GRCh37/hg19 Xp22.33-q28(chrX:168546-155233731)x1
HGVS:
NC_000023.10:g.(?_168546)_(155233731_?)del

Condition(s)

Synonyms:
none provided
Identifiers:
MedGen: C3661900

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Assertion and evidence details

Submission AccessionSubmitterReview Status
(Assertion method)
Clinical Significance
(Last evaluated)
OriginMethodCitations
SCV000990970Bionano Laboratories
no assertion criteria provided
Pathogenic
(Jun 26, 2018)
unknownclinical testing

Summary from all submissions

EthnicityOriginAffectedIndividualsFamiliesChromosomes testedNumber TestedFamily historyMethod
not providedunknownunknownnot providednot providednot providednot providednot providedclinical testing

Details of each submission

From Bionano Laboratories, SCV000990970.1

#EthnicityIndividualsChromosomes TestedFamily HistoryMethodCitations
1not providednot providednot providednot providedclinical testingnot provided
#SampleMethodObservation
OriginAffectedNumber testedTissuePurposeMethodIndividualsAllele frequencyFamiliesCo-occurrences
1unknownunknownnot providedBuccalnot providednot providednot providednot providednot provided

Last Updated: Sep 1, 2024