A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251055



Internal ID21308688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21693006..21701594hg38UCSC Ensembl
Outerchr11:21692916..21701937hg38UCSC Ensembl
Innerchr11:21714552..21723140hg19UCSC Ensembl
Outerchr11:21714462..21723483hg19UCSC Ensembl
Innerchr11:21671128..21679716hg18UCSC Ensembl
Outerchr11:21671038..21680059hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg389022
hg199022
hg189022
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170170
Supporting Variants
SamplesNGO_44
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251055
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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