A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1071081



Internal ID18976487
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:132952013..133106014hg38UCSC Ensembl
chr12:133528599..133682600hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38154002
hg19154002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3768255
SamplesKWP1
Known GenesZNF140, ZNF26, ZNF605, ZNF84
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1071081
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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