A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6468977



Internal ID21126530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94991501..94993200hg38UCSC Ensembl
chr11:94724665..94726364hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995538
Samples
Known GenesKDM4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6468977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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