A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695473



Internal ID15432125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:144628528..144676369hg38UCSC Ensembl
InnerchrX:143710050..143757890hg19UCSC Ensembl
InnerchrX:143517693..143565455hg18UCSC Ensembl
InnerchrX:143415547..143463309hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3847842
hg1947841
hg1847763
hg1747763
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)nssv695473
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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