A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527757



Internal ID15455050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:145380959..145486729hg38UCSC Ensembl
InnerchrX:144462477..144568247hg19UCSC Ensembl
InnerchrX:144270169..144375939hg18UCSC Ensembl
InnerchrX:144168023..144273793hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38105771
hg19105771
hg18105771
hg17105771
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704244
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527757
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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