A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688981



Internal ID15425633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:96537702..96579379hg38UCSC Ensembl
InnerchrX:95792701..95834378hg19UCSC Ensembl
InnerchrX:95679357..95721034hg18UCSC Ensembl
InnerchrX:95598846..95640523hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg3841678
hg1941678
hg1841678
hg1741678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519679
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv688981
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