A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700042



Internal ID15436694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6266293..6500018hg38UCSC Ensembl
InnerchrX:6184334..6418059hg19UCSC Ensembl
InnerchrX:6194334..6428059hg18UCSC Ensembl
InnerchrX:6044070..6277795hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38233726
hg19233726
hg18233726
hg17233726
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524163
Supporting Variants
Samples
Known GenesMIR4770
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700042
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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