A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526606



Internal ID15453899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:137028213..137057496hg38UCSC Ensembl
Innerchr2:137785783..137815066hg19UCSC Ensembl
Innerchr2:137502253..137531536hg18UCSC Ensembl
Innerchr2:137619515..137648798hg17UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3829284
hg1929284
hg1829284
hg1729284
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702926
Samples
Known GenesTHSD7B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526606
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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