A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035348



Internal ID18777879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82652403..82890613hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg18238211
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2641n100
Supporting Variantsnssv3718119
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, LOC388152, LOC440300, LOC642423, UBE2Q2P1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1035348
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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