A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv608422



Internal ID16049145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:130851633..130906219hg38UCSC Ensembl
Innerchr7:130536392..130590978hg19UCSC Ensembl
Innerchr7:130186932..130241518hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg3854587
hg1954587
hg1854587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1094521
Samples
Known GenesLOC646329, MIR29A, MIR29B1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv608422
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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