A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519041



Internal ID15099648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:108468676..108937930hg38UCSC Ensembl
InnerchrX:107711906..108181160hg19UCSC Ensembl
InnerchrX:107598562..108067816hg18UCSC Ensembl
InnerchrX:107518051..107987305hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg38469255
hg19469255
hg18469255
hg17469255
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696510
Samples
Known GenesCOL4A5, IRS4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519041
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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