A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694419



Internal ID15431071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28889785..28904210hg38UCSC Ensembl
InnerchrX:28907902..28922327hg19UCSC Ensembl
InnerchrX:28817823..28832248hg18UCSC Ensembl
InnerchrX:28667559..28681984hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg3814426
hg1914426
hg1814426
hg1714426
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)nssv694419
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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