A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv827591



Internal ID16121547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:44264601..44680343hg38UCSC Ensembl
Innerchr14:44733804..45149546hg19UCSC Ensembl
Innerchr14:43803554..44219296hg18UCSC Ensembl
Cytoband14q21.2
Allele length
AssemblyAllele length
hg38415743
hg19415743
hg18415743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv564681
Supporting Variants
Samples
Known GenesFSCB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv827591
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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