A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170298



Internal ID21314359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34500660..34508183hg38UCSC Ensembl
Outerchr11:34498031..34508611hg38UCSC Ensembl
Innerchr11:34522207..34529730hg19UCSC Ensembl
Outerchr11:34519578..34530158hg19UCSC Ensembl
Innerchr11:34478783..34486306hg18UCSC Ensembl
Outerchr11:34476154..34486734hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3810581
hg1910581
hg1810581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247061
SamplesNGO_16
Known GenesELF5
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170298
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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