A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516286



Internal ID15443579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:44725861..44795709hg38UCSC Ensembl
InnerchrX:44585107..44654955hg19UCSC Ensembl
InnerchrX:44470051..44539899hg18UCSC Ensembl
InnerchrX:44341361..44411209hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3869849
hg1969849
hg1869849
hg1769849
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705455, nssv667336, nssv660814, nssv703300, nssv659650, nssv656083
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516286
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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