A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565898



Internal ID16353307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101744061hg38UCSC Ensembl
Innerchr14:102174038..102210398hg19UCSC Ensembl
Innerchr14:101243791..101280151hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3836361
hg1936361
hg1836361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3924n54
Supporting Variantsnssv833757
Samples
Known GenesLINC00239
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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