A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102442



Internal ID20669482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:76164490..76265674hg38UCSC Ensembl
chr3:76213641..76314825hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38101185
hg19101185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361516
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102442
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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