A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038729



Internal ID19127948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..22283866hg38UCSC Ensembl
Innerchr15:20585976..22571817hg19UCSC Ensembl
Innerchr15:18845990..20073181hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg381903144
hg191985842
hg181227192
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2191n100
Supporting Variantsnssv3537378, nssv3537382, nssv3537380, nssv3537381, nssv3537379
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)nsv1038729
Frequency
Sample Size11257
Observed Gain3
Observed Loss2
Observed Complex0
Frequencyn/a


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