A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032205



Internal ID18774739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:132550902..133348828hg38UCSC Ensembl
Innerchr7:132235661..133033582hg19UCSC Ensembl
Innerchr7:131886201..132684122hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38797927
hg19797922
hg18797922
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662207
Samples
Known GenesCHCHD3, EXOC4, FLJ40288, MIR6133, PLXNA4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032205
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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