A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6471652



Internal ID21129205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31323801..31326400hg38UCSC Ensembl
chr12:31476735..31479334hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192732
Samples
Known GenesFAM60A, FLJ13224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6471652
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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