A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527239



Internal ID15454532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:25287353..25290619hg38UCSC Ensembl
InnerchrX:25305470..25308736hg19UCSC Ensembl
InnerchrX:25215391..25218657hg18UCSC Ensembl
InnerchrX:25065127..25068393hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg383267
hg193267
hg183267
hg173267
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703640
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527239
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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