A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045767



Internal ID18788298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313356..30515727hg38UCSC Ensembl
Innerchr15:30605559..30807930hg19UCSC Ensembl
Innerchr15:28392851..28595222hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38202372
hg19202372
hg18202372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2511n100
Supporting Variantsnssv3721561, nssv3546758, nssv3546753, nssv3546754, nssv3546756, nssv3546755, nssv3546757
Samples
Known GenesCHRFAM7A, LOC101059918
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045767
Frequency
Sample Size29084
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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