A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475313



Internal ID21132866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15613018..15618678hg38UCSC Ensembl
chr12:15765952..15771612hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385661
hg195661
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178012
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475313
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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