A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436941



Internal ID21094494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1575591..1576104hg38UCSC Ensembl
chr11:1596821..1597334hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg38514
hg19514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989409
Samples
Known GenesKRTAP5-AS1, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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