A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464785



Internal ID21122338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:101565071..101983757hg38UCSC Ensembl
chr11:101435802..101854488hg19UCSC Ensembl
Cytoband11q22.1
Allele length
AssemblyAllele length
hg38418687
hg19418687
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18186452
Samples
Known GenesANGPTL5, KIAA1377, TRPC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464785
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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