A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011765



Internal ID21921108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:100851711..100851797hg38UCSC Ensembl
chr6:101299587..101299673hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570707
Samples
Known GenesASCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011765
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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