A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672671



Internal ID15409323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:32462173..32473234hg38UCSC Ensembl
InnerchrX:32480290..32491351hg19UCSC Ensembl
InnerchrX:32390211..32401272hg18UCSC Ensembl
InnerchrX:32239947..32251008hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3811062
hg1911062
hg1811062
hg1711062
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)nssv672671
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