A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631875



Internal ID21823922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34845134..34845134hg38UCSC Ensembl
chr20:33432937..33432937hg19UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6111500
Supporting Variants
Samples
Known GenesGGT7
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631875
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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