A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18205570



Internal ID20772610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:156341401..156343000hg38UCSC Ensembl
chr2:157197913..157199512hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6348610
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18205570
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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