A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480724



Internal ID21138277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132591008..132612210hg38UCSC Ensembl
chr12:133167594..133188796hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3821203
hg1921203
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18180936
Samples
Known GenesLRCOL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480724
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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