A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565172



Internal ID21889527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93728065..93728065hg38UCSC Ensembl
chr7:93357377..93357377hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38315
hg19315
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6070514
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565172
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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