A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035269



Internal ID19124488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:45001..122957hg38UCSC Ensembl
Innerchr12:150430..232123hg19UCSC Ensembl
Innerchr12:20691..102384hg18UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3877957
hg1981694
hg1881694
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1328n100
Supporting Variantsnssv3503608
Samples
Known GenesIQSEC3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035269
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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