A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471164



Internal ID21128717
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 StatusM
Merged Variants
Supporting Variantsnssv17986654
Samples
Known GenesABCG4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471164
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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