A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511360



Internal ID15850785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155345842..155348443hg38UCSC Ensembl
Outerchr7:155345740..155350287hg38UCSC Ensembl
Innerchr7:155138542..155141146hg19UCSC Ensembl
Outerchr7:155138440..155142990hg19UCSC Ensembl
Innerchr7:154831298..154833899hg18UCSC Ensembl
Outerchr7:154831196..154835743hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg384548
hg194551
hg184548
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625901
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)nsv511360
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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