A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045541



Internal ID18788072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82652403..82886477hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg18234075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2641n100
Supporting Variantsnssv3554672, nssv3718118
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)nsv1045541
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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