A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043199



Internal ID19132418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20380723..20657723hg38UCSC Ensembl
Innerchr15:20585976..20863052hg19UCSC Ensembl
Innerchr15:18845990..19123066hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38277001
hg19277077
hg18277077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2244n100
Supporting Variantsnssv3714632, nssv3714630, nssv3714631
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)nsv1043199
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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