A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv690334



Internal ID15426986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:126796206..127212583hg38UCSC Ensembl
InnerchrX:125930189..126346566hg19UCSC Ensembl
InnerchrX:125757870..126174247hg18UCSC Ensembl
InnerchrX:125655724..126072101hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38416378
hg19416378
hg18416378
hg17416378
Variant TypeCNV gain
Copy Number
Allele State
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)nssv690334
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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