A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6476953



Internal ID21134506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:128382960..128383879hg38UCSC Ensembl
chr12:128867505..128868424hg19UCSC Ensembl
Cytoband12q24.32
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17997530
Samples
Known GenesTMEM132C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6476953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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