A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511443



Internal ID15850868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:127190362..127190834hg38UCSC Ensembl
Outerchr10:127188590..127190897hg38UCSC Ensembl
Innerchr10:128988626..128989098hg19UCSC Ensembl
Outerchr10:128986854..128989161hg19UCSC Ensembl
Innerchr10:128878616..128879088hg18UCSC Ensembl
Outerchr10:128876844..128879151hg18UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg382308
hg192308
hg182308
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626056
Samples1
Known GenesDOCK1, FAM196A
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv511443
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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