A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044767



Internal ID18787298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30483779..30795118hg38UCSC Ensembl
Innerchr15:30775982..31087321hg19UCSC Ensembl
Innerchr15:28563274..28874613hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38311340
hg19311340
hg18311340
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2526n100
Supporting Variantsnssv3721576
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044767
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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