A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091999



Internal ID15598499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102473462..102615025hg38UCSC Ensembl
Innerchr7:102113909..102255472hg19UCSC Ensembl
Innerchr7:101900914..102042692hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38141564
hg19141564
hg18141779
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv608004
Supporting Variants
Samples
Known GenesPOLR2J, POLR2J3, RASA4, RASA4B, SPDYE2, SPDYE2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091999
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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