A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147211



Internal ID19197149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:102885489..102885822hg38UCSC Ensembl
Outerchr10:104645246..104645579hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999984
SamplesKWB1
Known GenesAS3MT, C10orf32-ASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147211
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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