A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043624



Internal ID18786155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:90301813..90415770hg38UCSC Ensembl
Innerchr15:90845045..90959002hg19UCSC Ensembl
Innerchr15:88646049..88760006hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38113958
hg19113958
hg18113958
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2659n100
Supporting Variantsnssv3555213
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)nsv1043624
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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