A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525651



Internal ID15106258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:107966649..108001323hg38UCSC Ensembl
InnerchrX:107209879..107244553hg19UCSC Ensembl
InnerchrX:107096535..107131209hg18UCSC Ensembl
InnerchrX:107016024..107050698hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3834675
hg1934675
hg1834675
hg1734675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701806
Samples
Known GenesTEX13B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525651
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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