A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244064



Internal ID21302879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:105592740..105594295hg38UCSC Ensembl
Outerchr1:105591623..105596841hg38UCSC Ensembl
Innerchr1:106135362..106136917hg19UCSC Ensembl
Outerchr1:106134245..106139463hg19UCSC Ensembl
Innerchr1:105936885..105938440hg18UCSC Ensembl
Outerchr1:105935768..105940986hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg385219
hg195219
hg185219
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169608
Supporting Variants
SamplesMLY_2
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244064
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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