A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473753



Internal ID21131306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131867571..131879136hg38UCSC Ensembl
chr11:131737465..131749030hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3811566
hg1911566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987965
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473753
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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