A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565198



Internal ID16352607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:75054287..75058746hg38UCSC Ensembl
Innerchr14:75520990..75525449hg19UCSC Ensembl
Innerchr14:74590743..74595202hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg384460
hg194460
hg184460
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3778n54
Supporting Variantsnssv829550, nssv829549
Samples
Known GenesACYP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565198
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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