A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036686



Internal ID19125905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..21096875hg38UCSC Ensembl
Innerchr15:20586733..21302204hg19UCSC Ensembl
Innerchr15:18846747..19566863hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38715396
hg19715472
hg18720117
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3538720, nssv3538721
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)nsv1036686
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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