A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169587



Internal ID21313820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:89962617..89966887hg38UCSC Ensembl
Outerchr15:89959995..89971586hg38UCSC Ensembl
Innerchr15:90505849..90510119hg19UCSC Ensembl
Outerchr15:90503227..90514818hg19UCSC Ensembl
Innerchr15:88306853..88311123hg18UCSC Ensembl
Outerchr15:88304231..88315822hg18UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3811592
hg1911592
hg1811592
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242253
SamplesMLY_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169587
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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