A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv512463



Internal ID15851888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:896866..899943hg38UCSC Ensembl
Outerchr17:800106..803183hg19UCSC Ensembl
Outerchr17:746856..749933hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg383078
hg193078
hg183078
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625060
Samples1
Known GenesNXN
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv512463
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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