A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564887



Internal ID16352296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:62095928..62119235hg38UCSC Ensembl
Innerchr14:62562646..62585953hg19UCSC Ensembl
Innerchr14:61632399..61655706hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3823308
hg1923308
hg1823308
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149492
SamplesHGDP01418
Known GenesLINC00643, SYT16
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564887
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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