A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398178



Internal ID21055731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:60533427..60624267hg38UCSC Ensembl
chr5:59829254..59920094hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg3890841
hg1990841
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216244
Samples
Known GenesDEPDC1B, PART1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398178
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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