A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170225



Internal ID21314286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:18827010..19038370hg38UCSC Ensembl
Outerchr8:18824007..19038720hg38UCSC Ensembl
Innerchr8:18684520..18895880hg19UCSC Ensembl
Outerchr8:18681517..18896230hg19UCSC Ensembl
Innerchr8:18728800..18940160hg18UCSC Ensembl
Outerchr8:18725797..18940510hg18UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg38214714
hg19214714
hg18214714
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247143, nssv14250082
SamplesMLY_1, PML_2
Known GenesPSD3
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170225
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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