A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607743



Internal ID16048466
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88539385..90180497hg38UCSC Ensembl
Innerchr7:88168700..89809811hg19UCSC Ensembl
Innerchr7:88006636..89647747hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg381641113
hg191641112
hg181641112
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11493n54
Supporting Variantsnssv1089434
Samples
Known GenesC7orf62, DPY19L2P4, STEAP1, ZNF804B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607743
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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