A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677975



Internal ID15067941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:14599675..14641514hg38UCSC Ensembl
InnerchrX:14617797..14659636hg19UCSC Ensembl
InnerchrX:14527718..14569557hg18UCSC Ensembl
InnerchrX:14377454..14419293hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3841840
hg1941840
hg1841840
hg1741840
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520933
Supporting Variants
Samples
Known GenesGLRA2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677975
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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