A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169617



Internal ID21313428
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:22743174..22747803hg38UCSC Ensembl
Outerchr6:22741645..22751267hg38UCSC Ensembl
Innerchr6:22743403..22748032hg19UCSC Ensembl
Outerchr6:22741874..22751496hg19UCSC Ensembl
Innerchr6:22851382..22856011hg18UCSC Ensembl
Outerchr6:22849853..22859475hg18UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg389623
hg199623
hg189623
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249524
SamplesMLY_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169617
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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