A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17005964



Internal ID71588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156655799..156655850hg38UCSC Ensembl
chr7:156448493..156448544hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5405150
Supporting Variants
Samples
Known GenesRNF32
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17005964
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.008117


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