A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18097624



Internal ID20664664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:184699180..184706111hg38UCSC Ensembl
chr3:184416968..184423899hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg386932
hg196932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372354
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18097624
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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