A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608027



Internal ID16048750
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 StatusM
Merged Variantsdgv11544n54
Supporting Variantsnssv1092028
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)nsv608027
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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