A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv706004



Internal ID15442656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:95400783..95619871hg38UCSC Ensembl
InnerchrX:94655782..94874870hg19UCSC Ensembl
InnerchrX:94542438..94761526hg18UCSC Ensembl
InnerchrX:94461927..94681015hg17UCSC Ensembl
CytobandXq21.33
Allele length
AssemblyAllele length
hg38219089
hg19219089
hg18219089
hg17219089
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522611
Supporting Variants
Samples
Known GenesMIR548AE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv706004
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