A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248819



Internal ID21303553
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80566048..80579817hg38UCSC Ensembl
Outerchr6:80564619..80584624hg38UCSC Ensembl
Innerchr6:81275765..81289534hg19UCSC Ensembl
Outerchr6:81274336..81294341hg19UCSC Ensembl
Innerchr6:81332484..81346253hg18UCSC Ensembl
Outerchr6:81331055..81351060hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3820006
hg1920006
hg1820006
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169751
Supporting Variants
SamplesMLY_7
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248819
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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