A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527016



Internal ID15454309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:27692376..27704560hg38UCSC Ensembl
InnerchrX:27710493..27722677hg19UCSC Ensembl
InnerchrX:27620414..27632598hg18UCSC Ensembl
InnerchrX:27470150..27482334hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3812185
hg1912185
hg1812185
hg1712185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703391
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527016
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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