A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463914



Internal ID21121467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:76755737..76760161hg38UCSC Ensembl
chr11:76466781..76471205hg19UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg384425
hg194425
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994335
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463914
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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