A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242246



Internal ID21312401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4315300..4338058hg38UCSC Ensembl
Outerchr11:4315299..4363567hg38UCSC Ensembl
Innerchr11:4336530..4359288hg19UCSC Ensembl
Outerchr11:4336529..4384797hg19UCSC Ensembl
Innerchr11:4293106..4315864hg18UCSC Ensembl
Outerchr11:4293105..4341373hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3848269
hg1948269
hg1848269
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169696
Supporting Variants
SamplesSNI_17
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242246
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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