A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18090177



Internal ID20657217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67569262..67570588hg38UCSC Ensembl
chr2:67796394..67797720hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381327
hg191327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6345253
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18090177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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