A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626197



Internal ID15849730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:88546952..88547875hg38UCSC Ensembl
Outerchr16:88545605..88550289hg38UCSC Ensembl
Innerchr16:88613360..88614283hg19UCSC Ensembl
Outerchr16:88612013..88616697hg19UCSC Ensembl
Innerchr16:87140861..87141784hg18UCSC Ensembl
Outerchr16:87139514..87144198hg18UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg384685
hg194685
hg184685
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511571
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)nssv626197
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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