A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031937



Internal ID19121159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139880627..139905332hg38UCSC Ensembl
Innerchr8:140892871..140917576hg19UCSC Ensembl
Innerchr8:140962053..140986758hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3824706
hg1924706
hg1824706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690072
Samples
Known GenesTRAPPC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031937
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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