A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045457



Internal ID18787988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84129554..84509904hg38UCSC Ensembl
Innerchr15:84798306..85053135hg19UCSC Ensembl
Innerchr15:82589310..82854139hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38380351
hg19254830
hg18264830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2638n100
Supporting Variantsnssv3554631, nssv3554630
Samples
Known GenesDNM1P41, GOLGA6L4, GOLGA6L5P, 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)nsv1045457
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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