A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626588



Internal ID15850121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:195065244..195066341hg38UCSC Ensembl
Outerchr3:195064983..195066444hg38UCSC Ensembl
Innerchr3:194785973..194787070hg19UCSC Ensembl
Outerchr3:194785712..194787173hg19UCSC Ensembl
Innerchr3:196267262..196268359hg18UCSC Ensembl
Outerchr3:196267001..196268462hg18UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg381462
hg191462
hg181462
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511203
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)nssv626588
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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