A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607742



Internal ID16048465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88519150..90265948hg38UCSC Ensembl
Innerchr7:88148465..89895262hg19UCSC Ensembl
Innerchr7:87986401..89733198hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381746799
hg191746798
hg181746798
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11493n54
Supporting Variantsnssv1089433
Samples
Known GenesC7orf62, C7orf63, DPY19L2P4, STEAP1, STEAP2, ZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607742
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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