A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694577



Internal ID15431229
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28840673..28991133hg38UCSC Ensembl
InnerchrX:28858790..29009250hg19UCSC Ensembl
InnerchrX:28768711..28919171hg18UCSC Ensembl
InnerchrX:28618447..28768907hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg38150461
hg19150461
hg18150461
hg17150461
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521806
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694577
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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