A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524541



Internal ID15451834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:139081653..139126691hg38UCSC Ensembl
Innerchr8:140093896..140138934hg19UCSC Ensembl
Innerchr8:140163078..140208116hg18UCSC Ensembl
Innerchr8:140163078..140208116hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3845039
hg1945039
hg1845039
hg1745039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700491
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524541
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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