A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570963



Internal ID21763006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:102078562..102118754hg38UCSC Ensembl
chr6:102526437..102566629hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3840193
hg1940193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570963
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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