A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691200



Internal ID15427852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126206455..126224963hg38UCSC Ensembl
InnerchrX:125340438..125358946hg19UCSC Ensembl
InnerchrX:125168119..125186627hg18UCSC Ensembl
InnerchrX:125065973..125084481hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3818509
hg1918509
hg1818509
hg1718509
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520617
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv691200
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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