A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565897



Internal ID16353306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101727209hg38UCSC Ensembl
Innerchr14:102174038..102193546hg19UCSC Ensembl
Innerchr14:101243791..101263299hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3819509
hg1919509
hg1819509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3922n54
Supporting Variantsnssv833756
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565897
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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