A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625177



Internal ID15502027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:166975739..166976268hg38UCSC Ensembl
Outerchr5:166974202..166981659hg38UCSC Ensembl
Innerchr5:166402744..166403273hg19UCSC Ensembl
Outerchr5:166401207..166408664hg19UCSC Ensembl
Innerchr5:166335322..166335851hg18UCSC Ensembl
Outerchr5:166333785..166341242hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg387458
hg197458
hg187458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511295
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)nssv625177
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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