A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625012



Internal ID15501862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:3445157..3446989hg38UCSC Ensembl
Outerchr16:3495157..3496989hg19UCSC Ensembl
Outerchr16:3435158..3436990hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381833
hg191833
hg181833
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512420
Supporting Variants
Samples1
Known GenesNAA60
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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