A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692289



Internal ID15082255
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141381749..141396762hg38UCSC Ensembl
InnerchrX:140475913..140490920hg19UCSC Ensembl
InnerchrX:140303579..140318586hg18UCSC Ensembl
InnerchrX:140201433..140216440hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3815014
hg1915008
hg1815008
hg1715008
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv692289
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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