A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738259



Internal ID161925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155892881..155893014hg38UCSC Ensembl
chrX:155122544..155122677hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38134
hg19134
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422912
Supporting Variants
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738259
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000937


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