A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6477712



Internal ID21135265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:110737619..110738773hg38UCSC Ensembl
chr12:111175424..111176578hg19UCSC Ensembl
Cytoband12q24.11
Allele length
AssemblyAllele length
hg381155
hg191155
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996940
Samples
Known GenesPPP1CC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6477712
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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