A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565878



Internal ID16353287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101458153..101459426hg38UCSC Ensembl
Innerchr14:101924490..101925763hg19UCSC Ensembl
Innerchr14:100994243..100995516hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381274
hg191274
hg181274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3920n54
Supporting Variantsnssv833713
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565878
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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