A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6479810



Internal ID21137363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:129354137..129359281hg38UCSC Ensembl
chr12:129838682..129843826hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg385145
hg195145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997860
Samples
Known GenesTMEM132D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6479810
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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