A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569816



Internal ID21761859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90315095..90315095hg38UCSC Ensembl
chr7:89944409..89944409hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg385903
hg195903
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6065994
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569816
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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