A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477341



Internal ID21134894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:30619632..30619897hg38UCSC Ensembl
chr13:31193769..31194034hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007904
Samples
Known GenesUSPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477341
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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