A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701817



Internal ID15091783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150731781..150792646hg38UCSC Ensembl
InnerchrX:149900253..149961119hg19UCSC Ensembl
InnerchrX:149650911..149711777hg18UCSC Ensembl
InnerchrX:149570821..149631687hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3860866
hg1960867
hg1860867
hg1760867
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525661
Supporting Variants
Samples
Known GenesCD99L2, MTMR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701817
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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