A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669824



Internal ID15059790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51760517..51954513hg38UCSC Ensembl
InnerchrX:51503613..51697609hg19UCSC Ensembl
InnerchrX:51520353..51714349hg18UCSC Ensembl
InnerchrX:51336649..51530645hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg38193997
hg19193997
hg18193997
hg17193997
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)nssv669824
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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