A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565190



Internal ID16352599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75054287..75055662hg38UCSC Ensembl
Innerchr14:75520990..75522365hg19UCSC Ensembl
Innerchr14:74590743..74592118hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg381376
hg191376
hg181376
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3779n54
Supporting Variantsnssv829525, nssv829524
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565190
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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