A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564474



Internal ID16351883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41132802..41199131hg38UCSC Ensembl
Innerchr14:41602007..41668334hg19UCSC Ensembl
Innerchr14:40671757..40738084hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3866330
hg1966328
hg1866328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv826671, nssv826679, nssv826676, nssv826674, nssv826673, nssv826675, nssv826678, nssv826670, nssv826672, nssv826677, nssv826669, nssv826668
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564474
Frequency
Sample Size17421
Observed Gain0
Observed Loss12
Observed Complex0
Frequencyn/a


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