A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14250750



Internal ID21302856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:4926930..4952799hg38UCSC Ensembl
Outerchr11:4926918..4953934hg38UCSC Ensembl
Innerchr11:4948160..4974029hg19UCSC Ensembl
Outerchr11:4948148..4975164hg19UCSC Ensembl
Innerchr11:4904736..4930605hg18UCSC Ensembl
Outerchr11:4904724..4931740hg18UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3827017
hg1927017
hg1827017
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170219
Supporting Variants
SamplesMLY_2
Known GenesOR51A4
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14250750
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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