A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574221



Internal ID16361630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:2098562..2152006hg38UCSC Ensembl
Innerchr17:2001856..2055300hg19UCSC Ensembl
Innerchr17:1948606..2002050hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3853445
hg1953445
hg1853445
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866432
Samples
Known GenesSMG6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574221
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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