A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593618



Internal ID16381027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7582833..7635570hg38UCSC Ensembl
Innerchr4:7584560..7637297hg19UCSC Ensembl
Innerchr4:7635460..7688197hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3852738
hg1952738
hg1852738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv991223
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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