A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103596



Internal ID20670636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:66914989..66922135hg38UCSC Ensembl
chr3:66965413..66972559hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg387147
hg197147
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6361221
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103596
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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