A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045218



Internal ID18787749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90290495..90457213hg38UCSC Ensembl
Innerchr15:90833727..91000445hg19UCSC Ensembl
Innerchr15:88634731..88801449hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38166719
hg19166719
hg18166719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2658n100
Supporting Variantsnssv3555202
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)nsv1045218
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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