A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035608



Internal ID19124827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20609659hg38UCSC Ensembl
Innerchr15:20585976..20814965hg19UCSC Ensembl
Innerchr15:18845990..19074979hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38228937
hg19228990
hg18228990
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2249n100
Supporting Variantsnssv3537229, nssv3537232, nssv3537230, nssv3537227, nssv3537233, nssv3537231, nssv3537228
Samples
Known GenesGOLGA6L6, GOLGA8CP, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035608
Frequency
Sample Size11257
Observed Gain6
Observed Loss1
Observed Complex0
Frequencyn/a


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