A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565895



Internal ID16353304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101707701..101713702hg38UCSC Ensembl
Innerchr14:102174038..102180039hg19UCSC Ensembl
Innerchr14:101243791..101249792hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg386002
hg196002
hg186002
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833753, nssv833754, nssv833752, nssv833751, nssv833750
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565895
Frequency
Sample Size17421
Observed Gain2
Observed Loss3
Observed Complex0
Frequencyn/a


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