A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625712



Internal ID15502559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:99586704..99587354hg38UCSC Ensembl
Outerchr6:99583161..99597726hg38UCSC Ensembl
Innerchr6:100034580..100035230hg19UCSC Ensembl
Outerchr6:100031037..100045602hg19UCSC Ensembl
Innerchr6:100141301..100141951hg18UCSC Ensembl
Outerchr6:100137758..100152323hg18UCSC Ensembl
Cytoband6q16.2
Allele length
AssemblyAllele length
hg3814566
hg1914566
hg1814566
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511343
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)nssv625712
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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