A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036782



Internal ID19126001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20868184..22176259hg38UCSC Ensembl
Innerchr15:21073513..22464210hg19UCSC Ensembl
Innerchr15:19338171..19965574hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381308076
hg191390698
hg18627404
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n100
Supporting Variantsnssv3541349
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1036782
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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