A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097207



Internal ID20664247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:17138592..17145876hg38UCSC Ensembl
chr3:17180084..17187368hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg387285
hg197285
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366931
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097207
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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