A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564819



Internal ID16352228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48327100..48435698hg38UCSC Ensembl
Innerchr14:48796303..48904901hg19UCSC Ensembl
Innerchr14:47866053..47974651hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg38108599
hg19108599
hg18108599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3712n54
Supporting Variantsnssv827848, nssv827851, nssv827852, nssv827849, nssv827847, nssv827850
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564819
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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