A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565999



Internal ID16353408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103521722..103522729hg38UCSC Ensembl
Innerchr14:103988059..103989066hg19UCSC Ensembl
Innerchr14:103057812..103058819hg18UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg381008
hg191008
hg181008
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834356, nssv834357, nssv834358
Samples
Known GenesCKB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565999
Frequency
Sample Size17421
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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