A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv663390



Internal ID15400042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:33943647..34020958hg38UCSC Ensembl
InnerchrX:33961764..34039075hg19UCSC Ensembl
InnerchrX:33871685..33948996hg18UCSC Ensembl
InnerchrX:33721421..33798732hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3877312
hg1977312
hg1877312
hg1777312
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520379
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv663390
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