A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1054171



Internal ID18796702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82568764..82799325hg38UCSC Ensembl
Innerchr15:83237514..83468077hg19UCSC Ensembl
Innerchr15:81034569..81265131hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38230562
hg19230564
hg18230563
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2637n100
Supporting Variantsnssv3554619
Samples
Known GenesAP3B2, CPEB1, FSD2, LOC283692, LOC283693, LOC338963, SCARNA15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1054171
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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