A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395726



Internal ID21053279
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60608268..60613338hg38UCSC Ensembl
chr5:59904095..59909165hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg385071
hg195071
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216245
Samples
Known GenesDEPDC1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395726
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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