A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv595582



Internal ID16382991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:139194590..139268459hg38UCSC Ensembl
Innerchr4:140115744..140189613hg19UCSC Ensembl
Innerchr4:140335194..140409063hg18UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg3873870
hg1973870
hg1873870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1008209
Samples
Known GenesMGARP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv595582
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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