A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154637



Internal ID22085142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:82953142..82957416hg38UCSC Ensembl
Outerchr10:82951704..82958025hg38UCSC Ensembl
Innerchr10:84712898..84717172hg19UCSC Ensembl
Outerchr10:84711460..84717781hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg386322
hg196322
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4006060, nssv4006059
Samples
Known GenesNRG3
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154637
Frequency
Sample Size131
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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