A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18098979



Internal ID20666019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:176187025..176256216hg38UCSC Ensembl
chr3:175904813..175974004hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3869192
hg1969192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360447
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18098979
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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