A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041771



Internal ID19130990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32247324..32535323hg38UCSC Ensembl
Innerchr15:32539525..32827524hg19UCSC Ensembl
Innerchr15:30326817..30614816hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38288000
hg19288000
hg18288000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2547n100
Supporting Variantsnssv3721641
Samples
Known GenesGOLGA8K, GOLGA8O, ULK4P1, ULK4P2, ULK4P3, WHAMMP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1041771
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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