A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170064



Internal ID21314125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142018623..142033732hg38UCSC Ensembl
Outerchr8:142016479..142036153hg38UCSC Ensembl
Innerchr8:143099984..143115093hg19UCSC Ensembl
Outerchr8:143097840..143117514hg19UCSC Ensembl
Innerchr8:143097891..143113000hg18UCSC Ensembl
Outerchr8:143095747..143115421hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3819675
hg1919675
hg1819675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248102, nssv14246380, nssv14242197, nssv14248717
SamplesNGO_9, NGO_30, NGO_42, SNI_4
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170064
Frequency
Sample Size93
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer