A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625011



Internal ID15848547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:1372765..1374368hg38UCSC Ensembl
Outerchr16:1422766..1424369hg19UCSC Ensembl
Outerchr16:1362767..1364370hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381604
hg191604
hg181604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512419
Supporting Variants
Samples1
Known GenesUNKL
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625011
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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