A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701185



Internal ID15091151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51809788..51906728hg38UCSC Ensembl
InnerchrX:51552884..51649824hg19UCSC Ensembl
InnerchrX:51569624..51666564hg18UCSC Ensembl
InnerchrX:51385920..51482860hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3896941
hg1996941
hg1896941
hg1796941
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516643
Supporting Variants
Samples
Known GenesMAGED1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701185
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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