A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626135



Internal ID15849668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:71903837..71906451hg38UCSC Ensembl
Outerchr13:71902850..71915649hg38UCSC Ensembl
Innerchr13:72477975..72480589hg19UCSC Ensembl
Outerchr13:72476988..72489787hg19UCSC Ensembl
Innerchr13:71375976..71378590hg18UCSC Ensembl
Outerchr13:71374989..71387788hg18UCSC Ensembl
Cytoband13q21.33
Allele length
AssemblyAllele length
hg3812800
hg1912800
hg1812800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511515
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626135
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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