A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511445



Internal ID15850870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91873820..91874684hg38UCSC Ensembl
Outerchr10:91867401..91875784hg38UCSC Ensembl
Innerchr10:93633577..93634441hg19UCSC Ensembl
Outerchr10:93627158..93635541hg19UCSC Ensembl
Innerchr10:93623557..93624421hg18UCSC Ensembl
Outerchr10:93617138..93625521hg18UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg388384
hg198384
hg188384
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626058
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)nsv511445
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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