A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17986654



Internal ID20553694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:119159901..119161000hg38UCSC Ensembl
chr11:119030611..119031710hg19UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6471164
Supporting Variants
Samples
Known GenesABCG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17986654
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00015


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