A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442631



Internal ID21100184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:18700901..18710700hg38UCSC Ensembl
chr11:18722448..18732247hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17988669
Samples
Known GenesIGSF22, TMEM86A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442631
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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