A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593568



Internal ID16380977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7254893..7309672hg38UCSC Ensembl
Innerchr4:7256620..7311399hg19UCSC Ensembl
Innerchr4:7307521..7362300hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3854780
hg1954780
hg1854780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8943n54
Supporting Variantsnssv990879
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593568
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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