A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170268



Internal ID21314329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77541488..77544933hg38UCSC Ensembl
Outerchr6:77536901..77547932hg38UCSC Ensembl
Innerchr6:78251205..78254650hg19UCSC Ensembl
Outerchr6:78246618..78257649hg19UCSC Ensembl
Innerchr6:78307924..78311369hg18UCSC Ensembl
Outerchr6:78303337..78314368hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3811032
hg1911032
hg1811032
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252306
SamplesNGO_24
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170268
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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