A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6464272



Internal ID21121825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104954001..104989000hg38UCSC Ensembl
chr12:105347779..105382778hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3835000
hg1935000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196198
Samples
Known GenesC12orf45
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6464272
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer