A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408032



Internal ID21065585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60650769..60651089hg38UCSC Ensembl
chr5:59946596..59946916hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133142
Samples
Known GenesDEPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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