A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6347105



Internal ID21004658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:161197530..161288036hg38UCSC Ensembl
chr2:162054041..162144547hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg3890507
hg1990507
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207318
Samples
Known GenesTANK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6347105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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