A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242552



Internal ID21312826
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:93100309..93132579hg38UCSC Ensembl
Outerchr11:93096761..93142718hg38UCSC Ensembl
Innerchr11:92833475..92865745hg19UCSC Ensembl
Outerchr11:92829927..92875884hg19UCSC Ensembl
Innerchr11:92473123..92505393hg18UCSC Ensembl
Outerchr11:92469575..92515532hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3845958
hg1945958
hg1845958
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169571
Supporting Variants
SamplesSNI_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242552
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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