A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17739567



Internal ID163233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:20635488..20649488hg38UCSC Ensembl
chrX:20653606..20667606hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3814001
hg1914001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6137975
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17739567
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000627221


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