A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526179



Internal ID15106786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:26534790..26579076hg38UCSC Ensembl
Innerchr1:26861281..26905567hg19UCSC Ensembl
Innerchr1:26733868..26778154hg18UCSC Ensembl
Innerchr1:26545423..26589709hg17UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3844287
hg1944287
hg1844287
hg1744287
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702441
Samples
Known GenesMIR1976, RPS6KA1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526179
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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