A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564831



Internal ID16352240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48819161..48902680hg38UCSC Ensembl
Innerchr14:49288364..49371883hg19UCSC Ensembl
Innerchr14:48358114..48441633hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3883520
hg1983520
hg1883520
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3713n54
Supporting Variantsnssv827863
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564831
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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