A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626202



Internal ID15849735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:48475400..48476844hg38UCSC Ensembl
Outerchr16:48470453..48479070hg38UCSC Ensembl
Innerchr16:48509311..48510755hg19UCSC Ensembl
Outerchr16:48504364..48512981hg19UCSC Ensembl
Innerchr16:47066812..47068256hg18UCSC Ensembl
Outerchr16:47061865..47070482hg18UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg388618
hg198618
hg188618
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511575
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)nssv626202
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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