A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520450



Internal ID15447743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:53163143..53164859hg38UCSC Ensembl
Innerchr1:53628815..53630531hg19UCSC Ensembl
Innerchr1:53401403..53403119hg18UCSC Ensembl
Innerchr1:53340836..53342552hg17UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381717
hg191717
hg181717
hg171717
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv684433, nssv680733, nssv671581
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520450
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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