A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6012110



Internal ID21921453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17438062..17439432hg38UCSC Ensembl
chr6:17438293..17439663hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg381371
hg191371
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561345
Samples
Known GenesCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6012110
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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