A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566206



Internal ID16006929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105439736..105543235hg38UCSC Ensembl
Innerchr14:105906073..106009572hg19UCSC Ensembl
Innerchr14:104977118..105080617hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38103500
hg19103500
hg18103500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148637
Samples1780862275_A
Known GenesC14orf80, CRIP1, CRIP2, MTA1, TMEM121
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566206
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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