A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044668



Internal ID18787199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..22472558hg38UCSC Ensembl
Innerchr15:20262224..22752697hg19UCSC Ensembl
Innerchr15:18522238..20304061hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg382415588
hg192490474
hg181781824
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2179n100
Supporting Variantsnssv3538585
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L1, GOLGA6L6, GOLGA8CP, GOLGA8DP, HERC2P3, LOC646214, LOC727924, MIR4509-1, MIR4509-2, MIR4509-3, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044668
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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