A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565188



Internal ID16352597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75053362..75055876hg38UCSC Ensembl
Innerchr14:75520065..75522579hg19UCSC Ensembl
Innerchr14:74589818..74592332hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg382515
hg192515
hg182515
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829522
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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