A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248527



Internal ID21302707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:21701416..21721221hg38UCSC Ensembl
Outerchr11:21693006..21724212hg38UCSC Ensembl
Innerchr11:21722962..21742767hg19UCSC Ensembl
Outerchr11:21714552..21745758hg19UCSC Ensembl
Innerchr11:21679538..21699343hg18UCSC Ensembl
Outerchr11:21671128..21702334hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg3831207
hg1931207
hg1831207
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170170
Supporting Variants
SamplesMLY_17
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248527
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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