A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170121



Internal ID21314182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:90590585..90874828hg38UCSC Ensembl
Outerchr8:90584733..90877942hg38UCSC Ensembl
Innerchr8:91602813..91887056hg19UCSC Ensembl
Outerchr8:91596961..91890170hg19UCSC Ensembl
Innerchr8:91671989..91956232hg18UCSC Ensembl
Outerchr8:91666137..91959346hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38293210
hg19293210
hg18293210
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245418
SamplesMLY_9
Known GenesLINC01030, NECAB1, TMEM64
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170121
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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