A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827842



Internal ID16121798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48229326..48316156hg38UCSC Ensembl
Innerchr14:48698529..48785359hg19UCSC Ensembl
Innerchr14:47768279..47855109hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3886831
hg1986831
hg1886831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564813
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827842
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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