A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17009626



Internal ID74060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:39822512..39822557hg38UCSC Ensembl
chr8:39680031..39680076hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5539294
Supporting Variants
Samples
Known GenesADAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17009626
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.007649


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