A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350843



Internal ID21008396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231578191..231639778hg38UCSC Ensembl
chr2:232442902..232504489hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg3861588
hg1961588
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206210
Samples
Known GenesC2orf57
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350843
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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