A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052652



Internal ID18795183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90101186..90298961hg38UCSC Ensembl
Innerchr15:90644418..90842193hg19UCSC Ensembl
Innerchr15:88445422..88643197hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38197776
hg19197776
hg18197776
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555198
Samples
Known GenesCIB1, GDPGP1, IDH2, NGRN, SEMA4B, TTLL13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052652
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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