A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353106



Internal ID21010659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12652543..12655728hg38UCSC Ensembl
chr2:12792669..12795854hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg383186
hg193186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18076003
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353106
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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