A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351759



Internal ID21009312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:27783808..27786600hg38UCSC Ensembl
chr2:28006675..28009467hg19UCSC Ensembl
Cytoband2p23.2
Allele length
AssemblyAllele length
hg382793
hg192793
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087472
Samples
Known GenesRBKS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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