A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518142



Internal ID15445435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151739261..151751383hg38UCSC Ensembl
InnerchrX:150907733..150919855hg19UCSC Ensembl
InnerchrX:150658389..150670511hg18UCSC Ensembl
InnerchrX:150578301..150590423hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812123
hg1912123
hg1812123
hg1712123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695563
Samples
Known GenesCNGA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518142
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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