A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697488



Internal ID15434140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29268981..29287186hg38UCSC Ensembl
InnerchrX:29287098..29305303hg19UCSC Ensembl
InnerchrX:29197019..29215224hg18UCSC Ensembl
InnerchrX:29046755..29064960hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3818206
hg1918206
hg1818206
hg1718206
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)nssv697488
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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