A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244896



Internal ID21302449
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80568268..80579817hg38UCSC Ensembl
Outerchr6:80566395..80584624hg38UCSC Ensembl
Innerchr6:81277985..81289534hg19UCSC Ensembl
Outerchr6:81276112..81294341hg19UCSC Ensembl
Innerchr6:81334704..81346253hg18UCSC Ensembl
Outerchr6:81332831..81351060hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818230
hg1918230
hg1818230
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169751
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)nssv14244896
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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