A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521755



Internal ID15449048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:53370833..53399687hg38UCSC Ensembl
Innerchr6:53235631..53264485hg19UCSC Ensembl
Innerchr6:53343590..53372444hg18UCSC Ensembl
Innerchr6:53343590..53372444hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3828855
hg1928855
hg1828855
hg1728855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694522
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521755
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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