A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694749



Internal ID15084715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147228796..147380154hg38UCSC Ensembl
InnerchrX:146310314..146461672hg19UCSC Ensembl
InnerchrX:146118006..146269364hg18UCSC Ensembl
InnerchrX:146015860..146167218hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg38151359
hg19151359
hg18151359
hg17151359
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521982
Supporting Variants
Samples
Known GenesMIR506, MIR507, MIR508, MIR509-1, MIR509-2, MIR509-3, MIR510, MIR514A1, MIR514A2, MIR514A3, MIR514B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694749
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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