A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375506



Internal ID21033059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:51401550..51402644hg38UCSC Ensembl
chr3:51438981..51440078hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg381095
hg191098
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102889
Samples
Known GenesVPRBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375506
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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