A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18186605



Internal ID20753645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:62432201..62687400hg38UCSC Ensembl
chr13:63006334..63261533hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38255200
hg19255200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488936
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18186605
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00021


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