A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154549



Internal ID22085054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6936155..6946354hg38UCSC Ensembl
Outerchr10:6933714..6947777hg38UCSC Ensembl
Innerchr10:6978117..6988316hg19UCSC Ensembl
Outerchr10:6975676..6989739hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3814064
hg1914064
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv28n97
Supporting Variantsnssv4004586
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nsv1154549
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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