A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522926



Internal ID15450219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:167918030..167956910hg38UCSC Ensembl
Innerchr3:167635818..167674698hg19UCSC Ensembl
Innerchr3:169118512..169157392hg18UCSC Ensembl
Innerchr3:169118520..169157400hg17UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3838881
hg1938881
hg1838881
hg1738881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698588
Samples
Known GenesLOC646168
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522926
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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