A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6016180



Internal ID21925523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114266104..114266255hg38UCSC Ensembl
chr10:116025863..116026014hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38152
hg19152
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17592702
Samples
Known GenesVWA2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6016180
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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