A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493101



Internal ID21150654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:20228660..20260613hg38UCSC Ensembl
chr13:20802799..20834752hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3831954
hg1931954
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178164
Samples
Known GenesGJB6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493101
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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