A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347460



Internal ID21005013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74161609..74164478hg38UCSC Ensembl
chr2:74388736..74391605hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg382870
hg192870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207048
Samples
Known GenesMOB1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347460
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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