A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522792



Internal ID15103399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:105974807..106061636hg38UCSC Ensembl
Innerchr4:106895964..106982793hg19UCSC Ensembl
Innerchr4:107115413..107202242hg18UCSC Ensembl
Innerchr4:107253568..107340397hg17UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3886830
hg1986830
hg1886830
hg1786830
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698436
Samples
Known GenesTBCK
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522792
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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