A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049697



Internal ID19138916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20418941..21096875hg38UCSC Ensembl
Innerchr15:20624194..21302204hg19UCSC Ensembl
Innerchr15:18884208..19566863hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38677935
hg19678011
hg18682656
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2232n100
Supporting Variantsnssv3540861
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)nsv1049697
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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