A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17995539



Internal ID20562579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94995563..94996037hg38UCSC Ensembl
chr11:94728727..94729201hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38475
hg19475
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6469951
Supporting Variants
Samples
Known GenesKDM4D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17995539
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00039


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