A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701452



Internal ID15438104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29115026..29194087hg38UCSC Ensembl
InnerchrX:29133143..29212204hg19UCSC Ensembl
InnerchrX:29043064..29122125hg18UCSC Ensembl
InnerchrX:28892800..28971861hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3879062
hg1979062
hg1879062
hg1779062
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516364
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701452
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