A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136165



Internal ID18915598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132925914..133106014hg38UCSC Ensembl
Outerchr12:133502500..133682600hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg38180101
hg19180101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv917n106
Supporting Variantsnssv3989772
SamplesKWS2
Known GenesZNF140, ZNF26, ZNF605, ZNF84
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136165
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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