A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511354



Internal ID15850779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74122808..74123689hg38UCSC Ensembl
Outerchr6:74118966..74141337hg38UCSC Ensembl
Innerchr6:74832524..74833405hg19UCSC Ensembl
Outerchr6:74828682..74851053hg19UCSC Ensembl
Innerchr6:74889244..74890125hg18UCSC Ensembl
Outerchr6:74885402..74907773hg18UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3822372
hg1922372
hg1822372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625833
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)nsv511354
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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