A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342035



Internal ID20999588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:239765760..239771384hg38UCSC Ensembl
chr2:240687454..240693078hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385625
hg195625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208394
Samples
Known GenesLOC150935
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342035
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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