A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035817



Internal ID18778348
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:84192647..84550209hg38UCSC Ensembl
Innerchr15:84861399..85093440hg19UCSC Ensembl
Innerchr15:82652403..82894444hg18UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38357563
hg19232042
hg18242042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2638n100
Supporting Variantsnssv3555048, nssv3555047, nssv3718122, nssv3718121, nssv3718123, nssv3555045, nssv3718120, nssv3555046
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)nsv1035817
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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