A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035212



Internal ID19124431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:52703440..52738406hg38UCSC Ensembl
Innerchr15:52995637..53030603hg19UCSC Ensembl
Innerchr15:50782929..50817895hg18UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3834967
hg1934967
hg1834967
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2596n100
Supporting Variantsnssv3552406, nssv3552407
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)nsv1035212
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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