A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6346293



Internal ID21003846
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9128450..9350247hg38UCSC Ensembl
chr2:9268579..9490376hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38221798
hg19221798
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210668
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6346293
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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