A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704327



Internal ID15094293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:140214124..140814981hg38UCSC Ensembl
Innerchr3:139932966..140533823hg19UCSC Ensembl
Innerchr3:141415656..142016513hg18UCSC Ensembl
Innerchr3:141415664..142016521hg17UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg38600858
hg19600858
hg18600858
hg17600858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527831
Supporting Variants
Samples
Known GenesCLSTN2, CLSTN2-AS1, TRIM42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704327
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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