A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1092028



Internal ID15598528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102552586..102693659hg38UCSC Ensembl
Innerchr7:102193033..102334106hg19UCSC Ensembl
Innerchr7:101980132..102121342hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38141074
hg19141074
hg18141211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608027
Supporting Variants
Samples
Known GenesPOLR2J2, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B, UPK3BL
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1092028
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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