A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053382



Internal ID18795913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30438488..30638297hg38UCSC Ensembl
Innerchr15:30730691..30930500hg19UCSC Ensembl
Innerchr15:28517983..28717792hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38199810
hg19199810
hg18199810
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2524n100
Supporting Variantsnssv3547577, nssv3547576
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)nsv1053382
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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