A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244946



Internal ID21302574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2176090..2198736hg38UCSC Ensembl
Outerchr8:2173516..2201809hg38UCSC Ensembl
Innerchr8:2124280..2146289hg19UCSC Ensembl
Outerchr8:2121444..2149448hg19UCSC Ensembl
Innerchr8:2111687..2133696hg18UCSC Ensembl
Outerchr8:2108851..2136855hg18UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg3828294
hg1928005
hg1828005
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169893
Supporting Variants
SamplesMLY_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244946
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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