A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040994



Internal ID18783525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84992252..85041926hg38UCSC Ensembl
Innerchr15:85535483..85585157hg19UCSC Ensembl
Innerchr15:83336487..83386161hg18UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg3849675
hg1949675
hg1849675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3718141
Samples
Known GenesPDE8A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040994
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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