A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487282



Internal ID21144835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:27108632..27110409hg38UCSC Ensembl
chr13:27682769..27684546hg19UCSC Ensembl
Cytoband13q12.13
Allele length
AssemblyAllele length
hg381778
hg191778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007490
Samples
Known GenesUSP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487282
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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