A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245397



Internal ID21312057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4274526..4325579hg38UCSC Ensembl
Outerchr11:4254903..4331751hg38UCSC Ensembl
Innerchr11:4295756..4346809hg19UCSC Ensembl
Outerchr11:4276133..4352981hg19UCSC Ensembl
Innerchr11:4252332..4303385hg18UCSC Ensembl
Outerchr11:4232709..4309557hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3876849
hg1976849
hg1876849
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesSNI_15
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245397
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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