A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042566



Internal ID18785097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:82616277..82838909hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg18222633
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2641n100
Supporting Variantsnssv3554650, nssv3554649, nssv3554648
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)nsv1042566
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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