A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436720



Internal ID21094273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:4751884..4752500hg38UCSC Ensembl
chr11:4773114..4773730hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg38617
hg19617
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991156
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436720
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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