A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036462



Internal ID18778993
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82576576..82803755hg38UCSC Ensembl
Innerchr15:83245326..83472507hg19UCSC Ensembl
Innerchr15:81042381..81269561hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38227180
hg19227182
hg18227181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2637n100
Supporting Variantsnssv3718109
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)nsv1036462
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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