A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv511567



Internal ID15850992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35949228..35952207hg38UCSC Ensembl
Outerchr16:35877150..35957958hg38UCSC Ensembl
Innerchr16:35183599..35186578hg19UCSC Ensembl
Outerchr16:35111521..35192329hg19UCSC Ensembl
Innerchr16:35041100..35044079hg18UCSC Ensembl
Outerchr16:34969022..35049830hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg3880809
hg1980809
hg1880809
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv626193
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)nsv511567
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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