A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18184276



Internal ID20751316
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:81614870..81763292hg38UCSC Ensembl
chr13:82189005..82337427hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38148423
hg19148423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6477477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18184276
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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