A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351182



Internal ID21008735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145413379..145439788hg38UCSC Ensembl
chr2:146170947..146197356hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg3826410
hg1926410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351182
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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