A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6343357



Internal ID21000910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:43185596..43191934hg38UCSC Ensembl
chr2:43412735..43419073hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg386339
hg196339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088543
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6343357
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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