A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042355



Internal ID18784886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30158154..30807411hg38UCSC Ensembl
Innerchr15:30450357..31099614hg19UCSC Ensembl
Innerchr15:28237649..28886906hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38649258
hg19649258
hg18649258
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2505n100
Supporting Variantsnssv3546563
Samples
Known GenesARHGAP11B, CHRFAM7A, DKFZP434L187, GOLGA8H, LOC100288637, 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)nsv1042355
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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