A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566061



Internal ID16353470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104687768..104742230hg38UCSC Ensembl
Innerchr14:105154105..105208567hg19UCSC Ensembl
Innerchr14:104225150..104279612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3854463
hg1954463
hg1854463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3954n54
Supporting Variantsnssv1148714, nssv1148715
SamplesHGDP00558, 1798860108_A
Known GenesADSSL1, INF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566061
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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