A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449176



Internal ID21106729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:31302101..31311600hg38UCSC Ensembl
chr11:31323648..31333147hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg389500
hg199500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989646
Samples
Known GenesDCDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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