A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485512



Internal ID21143065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:63359151..63398761hg38UCSC Ensembl
chr13:63933284..63972894hg19UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg3839611
hg1939611
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178018
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485512
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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