A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565191



Internal ID16352600
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75054287..75055876hg38UCSC Ensembl
Innerchr14:75520990..75522579hg19UCSC Ensembl
Innerchr14:74590743..74592332hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381590
hg191590
hg181590
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3779n54
Supporting Variantsnssv829526
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565191
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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