A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341447



Internal ID20999000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:79210494..79227321hg38UCSC Ensembl
chr2:79437620..79454447hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3816828
hg1916828
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207700
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341447
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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