A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700707



Internal ID15090673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152414344..152436694hg38UCSC Ensembl
InnerchrX:151582816..151605166hg19UCSC Ensembl
InnerchrX:151333472..151355822hg18UCSC Ensembl
InnerchrX:151253384..151275734hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3822351
hg1922351
hg1822351
hg1722351
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516934
Supporting Variants
Samples
Known GenesGABRA3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700707
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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