A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036950



Internal ID18779481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82576576..82792509hg38UCSC Ensembl
Innerchr15:83245326..83461261hg19UCSC Ensembl
Innerchr15:81042381..81258315hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38215934
hg19215936
hg18215935
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2637n100
Supporting Variantsnssv3554620
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)nsv1036950
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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