A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529019



Internal ID15456312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:80239693..80264820hg38UCSC Ensembl
Innerchr4:81160847..81185974hg19UCSC Ensembl
Innerchr4:81379871..81404998hg18UCSC Ensembl
Innerchr4:81518026..81543153hg17UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg3825128
hg1925128
hg1825128
hg1725128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705730
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529019
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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