A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574425



Internal ID16361834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14635885..14672272hg38UCSC Ensembl
Innerchr17:14539202..14575589hg19UCSC Ensembl
Innerchr17:14479927..14516314hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3836388
hg1936388
hg1836388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149730
Samples1782681294_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574425
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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