A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525258



Internal ID15105865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70258925..70282204hg38UCSC Ensembl
InnerchrX:69478775..69502054hg19UCSC Ensembl
InnerchrX:69395500..69418779hg18UCSC Ensembl
InnerchrX:69261796..69285075hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3823280
hg1923280
hg1823280
hg1723280
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701357
Samples
Known GenesARR3, P2RY4, RAB41
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525258
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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