A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv590409



Internal ID16377818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:60946318..61055188hg38UCSC Ensembl
Innerchr3:60931990..61040860hg19UCSC Ensembl
Innerchr3:60907030..61015900hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38108871
hg19108871
hg18108871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1151901
SamplesHGDP00163
Known GenesFHIT
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv590409
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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