A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574375



Internal ID16361784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13280584..13325748hg38UCSC Ensembl
Innerchr17:13183901..13229065hg19UCSC Ensembl
Innerchr17:13124626..13169790hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3845165
hg1945165
hg1845165
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866928
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574375
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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