A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6037192



Internal ID21946535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:74139971..74140096hg38UCSC Ensembl
chr11:73851016..73851141hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38126
hg19126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597209
Samples
Known GenesC2CD3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6037192
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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