A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520087



Internal ID15447380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:121408071..121518605hg38UCSC Ensembl
InnerchrX:120541925..120652459hg19UCSC Ensembl
InnerchrX:120369606..120480140hg18UCSC Ensembl
InnerchrX:120267460..120377994hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38110535
hg19110535
hg18110535
hg17110535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv528n21
Supporting Variantsnssv697217
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520087
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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