A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18089956



Internal ID20656996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65159337..65162286hg38UCSC Ensembl
chr2:65386471..65389420hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg382950
hg192950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6355581
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18089956
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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