A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3936094



Internal ID21356163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:124350728..124350850hg38UCSC Ensembl
chrX:123484578..123484700hg19UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15200258
SamplesHG002
Known GenesSH2D1A
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3936094
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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