A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993842



Internal ID20560882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:6428577..6437175hg38UCSC Ensembl
chr11:6449807..6458405hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg388599
hg198599
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6446051
Supporting Variants
Samples
Known GenesHPX
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993842
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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