A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052982



Internal ID18795513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84159587..84402534hg38UCSC Ensembl
Innerchr15:84828339..84957232hg19UCSC Ensembl
Innerchr15:82619343..82748236hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38242948
hg19128894
hg18128894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2640n100
Supporting Variantsnssv3554659
Samples
Known GenesDNM1P41, GOLGA6L4, LOC100505679, LOC388152, LOC440300, LOC642423
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052982
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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