A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17701681



Internal ID125347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45656226..45657038hg38UCSC Ensembl
chr15:45948424..45949236hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5531195
Supporting Variants
Samples
Known GenesSQRDL
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17701681
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001405


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