A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474202



Internal ID21131755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30164322..30266885hg38UCSC Ensembl
chr12:30317255..30419818hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38102564
hg19102564
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18184180
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474202
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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