A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564460



Internal ID16351869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:40442154..40461772hg38UCSC Ensembl
Innerchr14:40911358..40930976hg19UCSC Ensembl
Innerchr14:39981108..40000726hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3819619
hg1919619
hg1819619
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3658n54
Supporting Variantsnssv1148696
SamplesNINDS_97
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564460
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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