A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574104



Internal ID16361513
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:947302..949747hg38UCSC Ensembl
Innerchr17:850542..852987hg19UCSC Ensembl
Innerchr17:797292..799737hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg382446
hg192446
hg182446
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv865852, nssv865851, nssv865853, nssv865854
Samples
Known GenesNXN
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574104
Frequency
Sample Size17421
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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