A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046512



Internal ID18789043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:32217691..32567645hg38UCSC Ensembl
Innerchr15:32509892..32859846hg19UCSC Ensembl
Innerchr15:30297184..30647138hg18UCSC Ensembl
Cytoband15q13.3
Allele length
AssemblyAllele length
hg38349955
hg19349955
hg18349955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2538n100
Supporting Variantsnssv3721639
Samples
Known GenesGOLGA8K, GOLGA8O, LOC100996255, 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)nsv1046512
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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