A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv594327



Internal ID16381736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:61321928..61408908hg38UCSC Ensembl
Innerchr4:62187646..62274626hg19UCSC Ensembl
Innerchr4:61870241..61957221hg18UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3886981
hg1986981
hg1886981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1000252
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv594327
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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