A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463382



Internal ID21120935
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102119074..102156407hg38UCSC Ensembl
chr12:102512852..102550185hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg3837334
hg1937334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996743
Samples
Known GenesPARPBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463382
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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