A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17698545



Internal ID122211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:22817876..22817941hg38UCSC Ensembl
chr15:23055127..23055192hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5497854
Supporting Variants
Samples
Known GenesNIPA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17698545
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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