A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698291



Internal ID15434943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29270532..29415237hg38UCSC Ensembl
InnerchrX:29288649..29433354hg19UCSC Ensembl
InnerchrX:29198570..29343275hg18UCSC Ensembl
InnerchrX:29048306..29193011hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38144706
hg19144706
hg18144706
hg17144706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521673
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698291
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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