A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246763



Internal ID21306683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30628421..30796274hg38UCSC Ensembl
Outerchr15:30621384..30807423hg38UCSC Ensembl
Innerchr15:30920624..31088477hg19UCSC Ensembl
Outerchr15:30913587..31099626hg19UCSC Ensembl
Innerchr15:28707916..28875769hg18UCSC Ensembl
Outerchr15:28700879..28886918hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38186040
hg19186040
hg18186040
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169498
Supporting Variants
SamplesNGO_3
Known GenesARHGAP11B, LOC100288637
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246763
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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