A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351396



Internal ID21008949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:33910752..34115434hg38UCSC Ensembl
chr2:34135819..34340501hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg38204683
hg19204683
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085979
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351396
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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