A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522151



Internal ID15102758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:181478542..181500662hg38UCSC Ensembl
Innerchr4:182399695..182421815hg19UCSC Ensembl
Innerchr4:182636689..182658809hg18UCSC Ensembl
Innerchr4:182774844..182796964hg17UCSC Ensembl
Cytoband4q34.3
Allele length
AssemblyAllele length
hg3822121
hg1922121
hg1822121
hg1722121
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694136
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522151
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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