A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525924



Internal ID15453217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:13254274..13256038hg38UCSC Ensembl
Innerchr4:13255898..13257662hg19UCSC Ensembl
Innerchr4:12864996..12866760hg18UCSC Ensembl
Innerchr4:12932167..12933931hg17UCSC Ensembl
Cytoband4p15.33
Allele length
AssemblyAllele length
hg381765
hg191765
hg181765
hg171765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702128
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525924
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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