A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104792



Internal ID20671832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96776301..96777200hg38UCSC Ensembl
chr3:96495145..96496044hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6370006
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.05745


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