A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18007900



Internal ID20574941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30445165..30448096hg38UCSC Ensembl
chr13:31019302..31022233hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg382932
hg192932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6487758
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18007900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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