A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18104955



Internal ID20671995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98915687..98920373hg38UCSC Ensembl
chr3:98634531..98639217hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg384687
hg194687
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6367963
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18104955
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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