A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv975377



Internal ID18610585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:30127513..30129781hg38UCSC Ensembl
Innerchr11:30149060..30151328hg19UCSC Ensembl
Innerchr11:30105636..30107904hg18UCSC Ensembl
Cytoband11p14.1
Allele length
AssemblyAllele length
hg382269
hg192269
hg182269
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2757566
SamplesHGDP00665
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv975377
Frequency
Sample Size10
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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