A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574395



Internal ID16361804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14286645..14294134hg38UCSC Ensembl
Innerchr17:14189962..14197451hg19UCSC Ensembl
Innerchr17:14130687..14138176hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg387490
hg197490
hg187490
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv867187, nssv867188
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574395
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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