A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18050603



Internal ID20617643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106028251..106278538hg38UCSC Ensembl
chr1:106570873..106821160hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38250288
hg19250288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330474
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18050603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00031


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