A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477213



Internal ID21134766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:37453972..37459661hg38UCSC Ensembl
chr13:38028109..38033798hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg385690
hg195690
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008434
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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