A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481688



Internal ID21139241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:66212297..66278693hg38UCSC Ensembl
chr13:66786429..66852825hg19UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg3866397
hg1966397
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18011596
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481688
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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