A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043789



Internal ID18786320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:55108674..55800256hg38UCSC Ensembl
Innerchr15:55400872..56092454hg19UCSC Ensembl
Innerchr15:53188164..53879746hg18UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38691583
hg19691583
hg18691583
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3552445
Samples
Known GenesC15orf65, CCPG1, DYX1C1, DYX1C1-CCPG1, MIR628, PIGB, PRTG, PYGO1, RAB27A, RSL24D1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043789
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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