A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574274



Internal ID16014997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4633926..4641837hg38UCSC Ensembl
Innerchr17:4537221..4545132hg19UCSC Ensembl
Innerchr17:4483970..4491881hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387912
hg197912
hg187912
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866562
Samples
Known GenesALOX15
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574274
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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