A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576062



Internal ID16016785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76385218..76386111hg38UCSC Ensembl
Innerchr17:74381299..74382192hg19UCSC Ensembl
Innerchr17:71892894..71893787hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38894
hg19894
hg18894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876209
Samples
Known GenesSPHK1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576062
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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