A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043031



Internal ID18785562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84158718..84397936hg38UCSC Ensembl
Innerchr15:84827470..84952634hg19UCSC Ensembl
Innerchr15:82618474..82743638hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38239219
hg19125165
hg18125165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2639n100
Supporting Variantsnssv3554657, nssv3554656
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)nsv1043031
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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