A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564847



Internal ID16352256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:54232948..54245496hg38UCSC Ensembl
Innerchr14:54699666..54712214hg19UCSC Ensembl
Innerchr14:53769416..53781964hg18UCSC Ensembl
Cytoband14q22.2
Allele length
AssemblyAllele length
hg3812549
hg1912549
hg1812549
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3715n54
Supporting Variantsnssv827891
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564847
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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