A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336430



Internal ID20993983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:67202501..67271800hg38UCSC Ensembl
chr2:67429633..67498932hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3869300
hg1969300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206967
Samples
Known GenesLOC644838
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336430
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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