A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574268



Internal ID16361677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4407344..4491875hg38UCSC Ensembl
Innerchr17:4310639..4395170hg19UCSC Ensembl
Innerchr17:4257388..4341919hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3884532
hg1984532
hg1884532
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866556
Samples
Known GenesSPNS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574268
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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