A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682974



Internal ID15419626
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32462173..32505725hg38UCSC Ensembl
InnerchrX:32480290..32523842hg19UCSC Ensembl
InnerchrX:32390211..32433763hg18UCSC Ensembl
InnerchrX:32239947..32283499hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3843553
hg1943553
hg1843553
hg1743553
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520320
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682974
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