A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042931



Internal ID19132150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20381480..22308242hg38UCSC Ensembl
Innerchr15:20586733..22673387hg19UCSC Ensembl
Innerchr15:18846747..20224751hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381926763
hg192086655
hg181378005
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2183n100
Supporting Variantsnssv3538760, nssv3714761, nssv3538761, nssv3538759
Samples
Known GenesCT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, LOC727924, NBEAP1, NF1P2, OR4M2, OR4N3P, OR4N4, POTEB, POTEB2, REREP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042931
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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