A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv509367



Internal ID15476865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117414490..117522633hg38UCSC Ensembl
Outerchr10:119174001..119282144hg19UCSC Ensembl
Outerchr10:119163991..119272134hg18UCSC Ensembl
Outerchr10:119163991..119272134hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg383636
hg193636
hg183636
hg173636
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv623781
SamplesNA18994
Known GenesEMX2OS
MethodOptical mapping
AnalysisSingle-molecule optical maps were assembled into genome-wide consensus maps. These consensus maps were compared to a restriction map generated from the NCBI b35 human genome reference sequence.
PlatformOptical Mapping
Comments
ReferenceTeague_et_al_2010
Pubmed ID20534489
Accession Number(s)nsv509367
Frequency
Sample Size4
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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