A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv593306



Internal ID16380715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:1493378..1521137hg38UCSC Ensembl
Innerchr4:1495105..1522864hg19UCSC Ensembl
Innerchr4:1464433..1492404hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3827760
hg1927760
hg1827972
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv987693, nssv987694
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv593306
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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