A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17567832



Internal ID21759875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35148983..35148983hg38UCSC Ensembl
chr6:35116760..35116760hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6079764
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17567832
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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