A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625013



Internal ID15848549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4719810..4722407hg38UCSC Ensembl
Outerchr16:4769811..4772408hg19UCSC Ensembl
Outerchr16:4709812..4712409hg18UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382598
hg192598
hg182598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512421
Supporting Variants
Samples1
Known GenesANKS3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625013
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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