A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522579



Internal ID15449872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28067121..28081458hg38UCSC Ensembl
InnerchrX:28085238..28099575hg19UCSC Ensembl
InnerchrX:27995159..28009496hg18UCSC Ensembl
InnerchrX:27844895..27859232hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3814338
hg1914338
hg1814338
hg1714338
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705966
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522579
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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