A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154579



Internal ID22085084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:45577424..45580787hg38UCSC Ensembl
Outerchr10:45574604..45584888hg38UCSC Ensembl
Innerchr10:46072872..46076235hg19UCSC Ensembl
Outerchr10:46070052..46080336hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3810285
hg1910285
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4004717, nssv4004736, nssv4004714, nssv4004732, nssv4004723, nssv4004728, nssv4004722, nssv4004716, nssv4004725, nssv4004721, nssv4004731, nssv4004718, nssv4004729, nssv4004715, nssv4004734, nssv4004735, nssv4004724, nssv4004720, nssv4004719, nssv4004726, nssv4004733, nssv4004713, nssv4004727, nssv4004730
Samples
Known GenesMARCH8
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154579
Frequency
Sample Size131
Observed Gain1
Observed Loss23
Observed Complex0
Frequencyn/a


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