A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036765



Internal ID19125984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:19599790..19633821hg38UCSC Ensembl
Innerchr12:19752724..19786755hg19UCSC Ensembl
Innerchr12:19643991..19678022hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3834032
hg1934032
hg1834032
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1401n100
Supporting Variantsnssv3505460
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036765
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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