A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683872



Internal ID15073838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:152202420..152414344hg38UCSC Ensembl
InnerchrX:151370892..151582816hg19UCSC Ensembl
InnerchrX:151121548..151333472hg18UCSC Ensembl
InnerchrX:151041460..151253384hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38211925
hg19211925
hg18211925
hg17211925
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)nssv683872
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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