A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566051



Internal ID16353460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104660017..104742230hg38UCSC Ensembl
Innerchr14:105126354..105208567hg19UCSC Ensembl
Innerchr14:104197399..104279612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3882214
hg1982214
hg1882214
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834432, nssv1148713
Samples1780862003_A
Known GenesADSSL1, INF2, MIR4710
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566051
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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