A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012909



Internal ID21922252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:955564..960653hg38UCSC Ensembl
chr6:955805..960891hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg385090
hg195087
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566622
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012909
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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