A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565971



Internal ID16006694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103100567..103135315hg38UCSC Ensembl
Innerchr14:103566904..103601652hg19UCSC Ensembl
Innerchr14:102636657..102671405hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg3834749
hg1934749
hg1834749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834318
Samples
Known GenesEXOC3L4, TNFAIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565971
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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