A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570623



Internal ID21762666
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:62305437..62305437hg38UCSC Ensembl
chr6:63015342..63015342hg19UCSC Ensembl
Cytoband6q11.1
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6073524
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570623
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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