A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700033



Internal ID15089999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:11723262..11798256hg38UCSC Ensembl
InnerchrX:11741382..11816375hg19UCSC Ensembl
InnerchrX:11651303..11726296hg18UCSC Ensembl
InnerchrX:11501039..11576032hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3874995
hg1974994
hg1874994
hg1774994
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524154
Supporting Variants
Samples
Known GenesMSL3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700033
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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