A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339350



Internal ID20996903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:201273384..201273761hg38UCSC Ensembl
chr2:202138107..202138484hg19UCSC Ensembl
Cytoband2q33.1
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208291
Samples
Known GenesCASP8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339350
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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