A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046117



Internal ID18788648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89683716..89765410hg38UCSC Ensembl
Innerchr15:90226947..90308641hg19UCSC Ensembl
Innerchr15:88027951..88109645hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3881695
hg1981695
hg1881695
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3555196
Samples
Known GenesMESP1, PEX11A, WDR93
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046117
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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