A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6345581



Internal ID21003134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:12746525..12747360hg38UCSC Ensembl
chr2:12886651..12887486hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg38836
hg19836
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207632
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6345581
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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