A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527181



Internal ID15454474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:38464035..38537676hg38UCSC Ensembl
Innerchr4:38465656..38539297hg19UCSC Ensembl
Innerchr4:38142051..38215692hg18UCSC Ensembl
Innerchr4:38288222..38361863hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3873642
hg1973642
hg1873642
hg1773642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv319n21
Supporting Variantsnssv703577
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527181
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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