A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18053176



Internal ID20620216
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17436601..17438700hg38UCSC Ensembl
chr1:17763097..17765196hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6331421
Supporting Variants
Samples
Known GenesRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18053176
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.02528


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