A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625901



Internal ID15849434
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 StatusS
Merged Variantsnsv511360
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)nssv625901
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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