A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461086



Internal ID21118639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1528483..1562123hg38UCSC Ensembl
chr12:1637649..1671289hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3833641
hg1933641
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195312
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461086
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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