A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705455



Internal ID15442107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44755902..44784369hg38UCSC Ensembl
InnerchrX:44615148..44643615hg19UCSC Ensembl
InnerchrX:44500092..44528559hg18UCSC Ensembl
InnerchrX:44371402..44399869hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3828468
hg1928468
hg1828468
hg1728468
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516286
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705455
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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