A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525786



Internal ID15106393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:17453781..17542854hg38UCSC Ensembl
InnerchrX:17471904..17560976hg19UCSC Ensembl
InnerchrX:17381825..17470897hg18UCSC Ensembl
InnerchrX:17231561..17320633hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3889074
hg1989073
hg1889073
hg1789073
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701962
Samples
Known GenesNHS
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525786
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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