A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565890



Internal ID16353299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101712843hg38UCSC Ensembl
Innerchr14:102174038..102179180hg19UCSC Ensembl
Innerchr14:101243791..101248933hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg385143
hg195143
hg185143
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3923n54
Supporting Variantsnssv833740
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565890
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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