A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040592



Internal ID18783123
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84156521..84397936hg38UCSC Ensembl
Innerchr15:84825273..84952634hg19UCSC Ensembl
Innerchr15:82616277..82743638hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38241416
hg19127362
hg18127362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2639n100
Supporting Variantsnssv3554646
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)nsv1040592
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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