A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521486



Internal ID15448779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:62513345..62547687hg38UCSC Ensembl
Innerchr4:63379063..63413405hg19UCSC Ensembl
Innerchr4:63061658..63096000hg18UCSC Ensembl
Innerchr4:63207829..63242171hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3834343
hg1934343
hg1834343
hg1734343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698097
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521486
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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