A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477477



Internal ID21135030
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 StatusM
Merged Variants
Supporting Variantsnssv18184276
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477477
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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