A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052679



Internal ID18795210
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30608663..30768969hg38UCSC Ensembl
Innerchr15:30900866..31061172hg19UCSC Ensembl
Innerchr15:28688158..28848464hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38160307
hg19160307
hg18160307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2530n100
Supporting Variantsnssv3547620
Samples
Known GenesARHGAP11B, GOLGA8H, LOC100288637
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052679
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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