A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593564



Internal ID16034287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7195666..7221054hg38UCSC Ensembl
Innerchr4:7197393..7222781hg19UCSC Ensembl
Innerchr4:7248294..7273682hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3825389
hg1925389
hg1825389
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv990876
Samples
Known GenesSORCS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593564
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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