A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339260



Internal ID20996813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218353333..218374621hg38UCSC Ensembl
chr2:219218056..219239344hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg3821289
hg1921289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085894
Samples
Known GenesC2orf62
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339260
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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