A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169835



Internal ID21313646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:127937888..127945252hg38UCSC Ensembl
Outerchr8:127935979..127950518hg38UCSC Ensembl
Innerchr8:128950134..128957498hg19UCSC Ensembl
Outerchr8:128948225..128962764hg19UCSC Ensembl
Innerchr8:129019316..129026680hg18UCSC Ensembl
Outerchr8:129017407..129031946hg18UCSC Ensembl
Cytoband8q24.21
Allele length
AssemblyAllele length
hg3814540
hg1914540
hg1814540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249034, nssv14247895
SamplesNGO_30, MLY_4
Known GenesPVT1, TMEM75
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169835
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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