A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042426



Internal ID18784957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30094196..30644082hg38UCSC Ensembl
Innerchr15:30386399..30936285hg19UCSC Ensembl
Innerchr15:28173691..28723577hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38549887
hg19549887
hg18549887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2495n100
Supporting Variantsnssv3546464
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, GOLGA8J, GOLGA8T, LOC101059918, ULK4P1, ULK4P2, ULK4P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042426
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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