A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050046



Internal ID19139265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20384762..20995359hg38UCSC Ensembl
Innerchr15:20590015..21200688hg19UCSC Ensembl
Innerchr15:18850029..19465347hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38610598
hg19610674
hg18615319
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3539565
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, 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)nsv1050046
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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