A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170297



Internal ID21314358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:116618444..116621018hg38UCSC Ensembl
Outerchr8:116612244..116623338hg38UCSC Ensembl
Innerchr8:117630683..117633257hg19UCSC Ensembl
Outerchr8:117624483..117635577hg19UCSC Ensembl
Innerchr8:117699864..117702438hg18UCSC Ensembl
Outerchr8:117693664..117704758hg18UCSC Ensembl
Cytoband8q23.3
Allele length
AssemblyAllele length
hg3811095
hg1911095
hg1811095
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14243989
SamplesMLY_3
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170297
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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