A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564347



Internal ID16351756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37089589..37120959hg38UCSC Ensembl
Innerchr14:37558794..37590164hg19UCSC Ensembl
Innerchr14:36628545..36659915hg18UCSC Ensembl
Cytoband14q13.3
Allele length
AssemblyAllele length
hg3831371
hg1931371
hg1831371
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825769
Samples
Known GenesSLC25A21
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564347
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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