A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049562



Internal ID19138781
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20406104..22033266hg38UCSC Ensembl
Innerchr15:20611357..22321217hg19UCSC Ensembl
Innerchr15:18871371..19822581hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381627163
hg191709861
hg18951211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2213n100
Supporting Variantsnssv3714808
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, 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)nsv1049562
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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