A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688899



Internal ID15425551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144638107..144724182hg38UCSC Ensembl
InnerchrX:143719628..143805703hg19UCSC Ensembl
InnerchrX:143527284..143613397hg18UCSC Ensembl
InnerchrX:143425138..143511251hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3886076
hg1986076
hg1886114
hg1786114
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516515
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688899
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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