A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351709



Internal ID21009262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201232450..201241113hg38UCSC Ensembl
chr2:202097173..202105836hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg388664
hg198664
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18084018
Samples
Known GenesCASP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351709
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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