A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517397



Internal ID15444690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:151278051..151307805hg38UCSC Ensembl
InnerchrX:150446523..150476277hg19UCSC Ensembl
InnerchrX:150197181..150226935hg18UCSC Ensembl
InnerchrX:150117091..150146845hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3829755
hg1929755
hg1829755
hg1729755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv691091, nssv675658, nssv666537, nssv673196, nssv689477, nssv697321, nssv651900
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517397
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer