A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876247



Internal ID15823517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77272529..77281529hg38UCSC Ensembl
Innerchr17:75268611..75277611hg19UCSC Ensembl
Innerchr17:72780206..72789206hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg389001
hg199001
hg189001
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576090
Supporting Variants
Samples
Known GenesSEPT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876247
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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