A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565669



Internal ID16353078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:98711970..98727250hg38UCSC Ensembl
Innerchr14:99178307..99193587hg19UCSC Ensembl
Innerchr14:98248060..98263340hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg3815281
hg1915281
hg1815281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3871n54
Supporting Variantsnssv832757, nssv832758, nssv832750, nssv832752, nssv832751, nssv832754, nssv832753, nssv832759, nssv832755, nssv832756
Samples
Known GenesC14orf177
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565669
Frequency
Sample Size17421
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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