A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036474



Internal ID19125693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:15159975..15187960hg38UCSC Ensembl
Innerchr11:15181521..15209506hg19UCSC Ensembl
Innerchr11:15138097..15166082hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg3827986
hg1927986
hg1827986
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3708518
Samples
Known GenesINSC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036474
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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