A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17738260



Internal ID161926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155894068..155894315hg38UCSC Ensembl
chrX:155123731..155123978hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38248
hg19248
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418006
Supporting Variants
Samples
Known GenesVAMP7
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17738260
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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