A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17699774



Internal ID123440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:42320628..42320666hg38UCSC Ensembl
chr15:42612826..42612864hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5543309
Supporting Variants
Samples
Known GenesGANC
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17699774
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.002655


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