A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17578685



Internal ID21770728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61202586..61202586hg38UCSC Ensembl
chr8:62115145..62115145hg19UCSC Ensembl
Cytoband8q12.2
Allele length
AssemblyAllele length
hg382991
hg192991
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6077985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17578685
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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