A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527447



Internal ID15454740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:108873603..108941145hg38UCSC Ensembl
Innerchr1:109416225..109483767hg19UCSC Ensembl
Innerchr1:109217748..109285290hg18UCSC Ensembl
Innerchr1:109128267..109195809hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3867543
hg1967543
hg1867543
hg1767543
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n21
Supporting Variantsnssv703888
Samples
Known GenesCLCC1, GPSM2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527447
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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