A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040878



Internal ID18783409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30450930..30644082hg38UCSC Ensembl
Innerchr15:30743133..30936285hg19UCSC Ensembl
Innerchr15:28530425..28723577hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38193153
hg19193153
hg18193153
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2524n100
Supporting Variantsnssv3547593
Samples
Known GenesARHGAP11B, GOLGA8H, 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)nsv1040878
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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