A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511547



Internal ID15504286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:77038445..77040265hg38UCSC Ensembl
Outerchr15:77035928..77045307hg38UCSC Ensembl
Innerchr15:77330786..77332606hg19UCSC Ensembl
Outerchr15:77328269..77337649hg19UCSC Ensembl
Innerchr15:75117841..75119661hg18UCSC Ensembl
Outerchr15:75115324..75124704hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg389380
hg199381
hg189381
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626171
Samples1
Known GenesPSTPIP1, TSPAN3
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511547
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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