A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351418



Internal ID21008971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75007904..75032717hg38UCSC Ensembl
chr2:75235031..75259844hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3824814
hg1924814
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18207649
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351418
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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