A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18105232



Internal ID20672272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77990697..77991248hg38UCSC Ensembl
chr3:78039848..78040399hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38552
hg19552
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372084
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18105232
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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