A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207632



Internal ID20774672
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 StatusS
Merged Variantsnsv6345581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207632
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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