A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036624



Internal ID19125843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20880182..22236602hg38UCSC Ensembl
Innerchr15:21085511..22524553hg19UCSC Ensembl
Innerchr15:19350185..20025917hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381356421
hg191439043
hg18675733
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2332n100
Supporting Variantsnssv3716102
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)nsv1036624
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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