A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519630



Internal ID15446923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:39199452..39209346hg38UCSC Ensembl
InnerchrX:39058705..39068599hg19UCSC Ensembl
InnerchrX:38943649..38953543hg18UCSC Ensembl
InnerchrX:38814921..38824815hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg389895
hg199895
hg189895
hg179895
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv694338
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519630
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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