A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657732



Internal ID15047698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152289446..152511752hg38UCSC Ensembl
InnerchrX:151457918..151680224hg19UCSC Ensembl
InnerchrX:151208574..151430880hg18UCSC Ensembl
InnerchrX:151128486..151350792hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38222307
hg19222307
hg18222307
hg17222307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516934
Supporting Variants
Samples
Known GenesGABRA3, MIR105-1, MIR105-2, MIR767
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657732
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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