A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350357



Internal ID21007910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:31739939..31748801hg38UCSC Ensembl
chr2:31965008..31973870hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg388863
hg198863
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085269
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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