A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035177



Internal ID19124396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..22100273hg38UCSC Ensembl
Innerchr15:20590015..22388224hg19UCSC Ensembl
Innerchr15:18850029..19889588hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381715512
hg191798210
hg181039560
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2238n100
Supporting Variantsnssv3539586, nssv3539585
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, 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)nsv1035177
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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