A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17569637



Internal ID21761680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:37501112..37501210hg38UCSC Ensembl
chr6:37468888..37468986hg19UCSC Ensembl
Cytoband6p21.2
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6013011
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17569637
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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