A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047880



Internal ID18790411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30313356..30472412hg38UCSC Ensembl
Innerchr15:30605559..30764615hg19UCSC Ensembl
Innerchr15:28392851..28551907hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38159057
hg19159057
hg18159057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2513n100
Supporting Variantsnssv3721559
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)nsv1047880
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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