A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593561



Internal ID16034284
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7153016..7218206hg38UCSC Ensembl
Innerchr4:7154743..7219933hg19UCSC Ensembl
Innerchr4:7205644..7270834hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3865191
hg1965191
hg1865191
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv990875
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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