A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344140



Internal ID21001693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:115579804..117125256hg38UCSC Ensembl
chr2:116337380..117882832hg19UCSC Ensembl
Cytoband2q14.1
Allele length
AssemblyAllele length
hg381545453
hg191545453
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206515
Samples
Known GenesDPP10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344140
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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