A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517568



Internal ID15444861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:125608357..125947509hg38UCSC Ensembl
InnerchrX:124742354..125081491hg19UCSC Ensembl
InnerchrX:124570035..124909172hg18UCSC Ensembl
InnerchrX:124467889..124807026hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38339153
hg19339138
hg18339138
hg17339138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv682832, nssv670844, nssv652388, nssv686048
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517568
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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