A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247191



Internal ID21305991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:26008032..26016943hg38UCSC Ensembl
Outerchr6:26005233..26018984hg38UCSC Ensembl
Innerchr6:26008260..26017171hg19UCSC Ensembl
Outerchr6:26005461..26019212hg19UCSC Ensembl
Innerchr6:26116239..26125150hg18UCSC Ensembl
Outerchr6:26113440..26127191hg18UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg3813752
hg1913752
hg1813752
Variant TypeCNV duplication
Copy Number4
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169862
Supporting Variants
SamplesNGO_24
Known GenesHIST1H1A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247191
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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