A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350351



Internal ID21007904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:61674278..61707060hg38UCSC Ensembl
chr2:61901413..61934195hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3832783
hg1932783
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18206374
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350351
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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