A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574373



Internal ID16361782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:13273495..13358124hg38UCSC Ensembl
Innerchr17:13176812..13261441hg19UCSC Ensembl
Innerchr17:13117537..13202166hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3884630
hg1984630
hg1884630
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866926
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574373
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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