A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169936



Internal ID21313997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80151846..80290496hg38UCSC Ensembl
Outerchr6:80150355..80295205hg38UCSC Ensembl
Innerchr6:80861563..81000213hg19UCSC Ensembl
Outerchr6:80860072..81004922hg19UCSC Ensembl
Innerchr6:80918282..81056932hg18UCSC Ensembl
Outerchr6:80916791..81061641hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg38144851
hg19144851
hg18144851
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244370
SamplesMLY_14
Known GenesBCKDHB
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169936
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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