A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461901



Internal ID21119454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:107755001..107783900hg38UCSC Ensembl
chr12:108148778..108177677hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg3828900
hg1928900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18196253
Samples
Known GenesASCL4, PRDM4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461901
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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