A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593567



Internal ID16380976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7254893..7295779hg38UCSC Ensembl
Innerchr4:7256620..7297506hg19UCSC Ensembl
Innerchr4:7307521..7348407hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3840887
hg1940887
hg1840887
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv8943n54
Supporting Variantsnssv990878
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593567
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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