A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18094765



Internal ID20661805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160395997..160399027hg38UCSC Ensembl
chr3:160113785..160116815hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg383031
hg193031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6358984
Supporting Variants
Samples
Known GenesIFT80
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18094765
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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