A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525223



Internal ID15105830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:40664921..40754042hg38UCSC Ensembl
InnerchrX:40524173..40613295hg19UCSC Ensembl
InnerchrX:40409117..40498239hg18UCSC Ensembl
InnerchrX:40280427..40369549hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3889122
hg1989123
hg1889123
hg1789123
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701311
Samples
Known GenesMED14
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525223
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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