A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043182



Internal ID18785713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30201146..30633390hg38UCSC Ensembl
Innerchr15:30493349..30925593hg19UCSC Ensembl
Innerchr15:28280641..28712885hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38432245
hg19432245
hg18432245
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2503n100
Supporting Variantsnssv3546617, nssv3546618, nssv3546619
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, LOC101059918, 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)nsv1043182
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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