A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv655128



Internal ID15391780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28931644..29195270hg38UCSC Ensembl
InnerchrX:28949761..29213387hg19UCSC Ensembl
InnerchrX:28859682..29123308hg18UCSC Ensembl
InnerchrX:28709418..28973044hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38263627
hg19263627
hg18263627
hg17263627
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)nssv655128
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