A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1091903



Internal ID15945089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:102040283..102088685hg38UCSC Ensembl
Innerchr7:101683563..101731965hg19UCSC Ensembl
Innerchr7:101470283..101518685hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3848403
hg1948403
hg1848403
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv607985
Supporting Variants
Samples
Known GenesCUX1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1091903
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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