A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566132



Internal ID21758175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156941031..156941031hg38UCSC Ensembl
chr7:156733725..156733725hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065425
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566132
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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