A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039559



Internal ID19128778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:61208547..61400008hg38UCSC Ensembl
Innerchr12:61602328..61793789hg19UCSC Ensembl
Innerchr12:59888595..60080056hg18UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38191462
hg19191462
hg18191462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3523657
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)nsv1039559
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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