A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525092



Internal ID15105699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:8998487..9020907hg38UCSC Ensembl
Innerchr1:9058546..9080966hg19UCSC Ensembl
Innerchr1:8981133..9003553hg18UCSC Ensembl
Innerchr1:8992812..9015232hg17UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3822421
hg1922421
hg1822421
hg1722421
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701151
Samples
Known GenesSLC2A7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525092
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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