A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6462597



Internal ID21120150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:81202047..81209095hg38UCSC Ensembl
chr11:80913090..80920138hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg387049
hg197049
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994492
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6462597
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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