A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526302



Internal ID15106909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:11723262..11864046hg38UCSC Ensembl
InnerchrX:11741382..11882165hg19UCSC Ensembl
InnerchrX:11651303..11792086hg18UCSC Ensembl
InnerchrX:11501039..11641822hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg38140785
hg19140784
hg18140784
hg17140784
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702584
Samples
Known GenesMSL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526302
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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