A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523165



Internal ID15103772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:124467033..124512492hg38UCSC Ensembl
InnerchrX:123600883..123646342hg19UCSC Ensembl
InnerchrX:123428564..123474023hg18UCSC Ensembl
InnerchrX:123326418..123371877hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3845460
hg1945460
hg1845460
hg1745460
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698877
Samples
Known GenesTENM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523165
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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