A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154663



Internal ID22085168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:124381580..124385663hg38UCSC Ensembl
Outerchr10:124377391..124386157hg38UCSC Ensembl
Innerchr10:126070149..126074232hg19UCSC Ensembl
Outerchr10:126065960..126074726hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388767
hg198767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4005519
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154663
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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