A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169571



Internal ID21313804
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14246294, nssv14242552
SamplesSNI_10, SNI_5
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169571
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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