A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703610



Internal ID15440262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:6485999..6486978hg38UCSC Ensembl
Innerchr4:6487726..6488705hg19UCSC Ensembl
Innerchr4:6538627..6539606hg18UCSC Ensembl
Innerchr4:6605798..6606777hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38980
hg19980
hg18980
hg17980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527210
Supporting Variants
Samples
Known GenesPPP2R2C
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703610
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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