A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250453



Internal ID21304493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80574472..80579817hg38UCSC Ensembl
Outerchr6:80568270..80584624hg38UCSC Ensembl
Innerchr6:81284189..81289534hg19UCSC Ensembl
Outerchr6:81277987..81294341hg19UCSC Ensembl
Innerchr6:81340908..81346253hg18UCSC Ensembl
Outerchr6:81334706..81351060hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3816355
hg1916355
hg1816355
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169751
Supporting Variants
SamplesNGO_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250453
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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