A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699055



Internal ID15435707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:29518008..29629904hg38UCSC Ensembl
InnerchrX:29536125..29648021hg19UCSC Ensembl
InnerchrX:29446046..29557942hg18UCSC Ensembl
InnerchrX:29295782..29407678hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg38111897
hg19111897
hg18111897
hg17111897
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523313
Supporting Variants
Samples
Known GenesIL1RAPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699055
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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