A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16914669



Internal ID10528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:71840664..71840664hg38UCSC Ensembl
chr2:72067794..72067794hg19UCSC Ensembl
Cytoband2p13.2
Allele length
AssemblyAllele length
hg38253
hg19253
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5544642
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16914669
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001721


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