A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524827



Internal ID15452120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22299406..22310521hg38UCSC Ensembl
InnerchrX:22317523..22328638hg19UCSC Ensembl
InnerchrX:22227444..22238559hg18UCSC Ensembl
InnerchrX:22077180..22088295hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3811116
hg1911116
hg1811116
hg1711116
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700826
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524827
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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