A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638127



Internal ID21830174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37016012..37016012hg38UCSC Ensembl
chr21:38388312..38388312hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg38325
hg19325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107756
Supporting Variants
Samples
Known GenesRIPPLY3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638127
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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