A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695801



Internal ID15432453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18143140..18173801hg38UCSC Ensembl
Innerchr11:18164687..18195348hg19UCSC Ensembl
Innerchr11:18121263..18151924hg18UCSC Ensembl
Innerchr11:18121263..18151924hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3830662
hg1930662
hg1830662
hg1730662
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518373
Supporting Variants
Samples
Known GenesMRGPRX4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695801
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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