A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470921



Internal ID21128474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7007137..7007588hg38UCSC Ensembl
chr12:7114442..7114893hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38452
hg19452
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18195550
Samples
Known GenesLPCAT3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470921
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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