A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525785



Internal ID15453078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:10490835..10573630hg38UCSC Ensembl
InnerchrX:10458875..10541670hg19UCSC Ensembl
InnerchrX:10418875..10501670hg18UCSC Ensembl
InnerchrX:10268611..10351406hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3882796
hg1982796
hg1882796
hg1782796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv500n21
Supporting Variantsnssv701961
Samples
Known GenesMID1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525785
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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