A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038878



Internal ID18781409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20942515..22023848hg38UCSC Ensembl
Innerchr15:21147844..22311799hg19UCSC Ensembl
Innerchr15:19412503..19813163hg18UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg381081334
hg191163956
hg18400661
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2347n100
Supporting Variantsnssv3541486, nssv3541487
Samples
Known GenesCT60, CXADRP2, LOC646214, LOC727924, 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)nsv1038878
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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