A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574267



Internal ID16361676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4395961..4451053hg38UCSC Ensembl
Innerchr17:4299256..4354348hg19UCSC Ensembl
Innerchr17:4246005..4301097hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3855093
hg1955093
hg1855093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866555
Samples
Known GenesSPNS3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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