A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17566561



Internal ID21758604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37428008..37428062hg38UCSC Ensembl
chr6:37395784..37395838hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6015883
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17566561
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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