A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6437128



Internal ID21094681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:2212082..2356488hg38UCSC Ensembl
chr11:2233312..2377718hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38144407
hg19144407
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18188083
Samples
Known GenesASCL2, C11orf21, CD81-AS1, TSPAN32
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6437128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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