A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683848



Internal ID15420500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126812220..126829262hg38UCSC Ensembl
InnerchrX:125946203..125963245hg19UCSC Ensembl
InnerchrX:125773884..125790926hg18UCSC Ensembl
InnerchrX:125671738..125688780hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3817043
hg1917043
hg1817043
hg1717043
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519509
Supporting Variants
Samples
Known GenesCXorf64
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683848
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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