A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv529018



Internal ID15456311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:152700377..152719461hg38UCSC Ensembl
Innerchr4:153621529..153640613hg19UCSC Ensembl
Innerchr4:153840979..153860063hg18UCSC Ensembl
Innerchr4:153979134..153998218hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3819085
hg1919085
hg1819085
hg1719085
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705729
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv529018
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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