A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039495



Internal ID18782026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90305211..90404314hg38UCSC Ensembl
Innerchr15:90848443..90947546hg19UCSC Ensembl
Innerchr15:88649447..88748550hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3899104
hg1999104
hg1899104
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2659n100
Supporting Variantsnssv3555216, nssv3555214, nssv3555215
Samples
Known GenesGABARAPL3, IQGAP1, ZNF774
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039495
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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