A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698127



Internal ID15088093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31213555..31236885hg38UCSC Ensembl
InnerchrX:31231672..31255002hg19UCSC Ensembl
InnerchrX:31141593..31164923hg18UCSC Ensembl
InnerchrX:30991329..31014659hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3823331
hg1923331
hg1823331
hg1723331
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521510
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698127
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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