A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564963



Internal ID16352372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:68749695..68763363hg38UCSC Ensembl
Innerchr14:69216412..69230080hg19UCSC Ensembl
Innerchr14:68286165..68299833hg18UCSC Ensembl
Cytoband14q24.1
Allele length
AssemblyAllele length
hg3813669
hg1913669
hg1813669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149500
SamplesHGDP00777
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564963
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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