A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739376



Internal ID163042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:14831837..14838078hg38UCSC Ensembl
chrX:14849959..14856200hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg386242
hg196242
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5415181
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739376
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0024974


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