A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250352



Internal ID21304824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:141847034..141852090hg38UCSC Ensembl
Outerchr8:141844777..141863858hg38UCSC Ensembl
Innerchr8:142928395..142933451hg19UCSC Ensembl
Outerchr8:142926138..142945219hg19UCSC Ensembl
Innerchr8:142926302..142931358hg18UCSC Ensembl
Outerchr8:142924045..142943126hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3819082
hg1919082
hg1819082
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169397
Supporting Variants
SamplesNGO_16
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250352
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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