A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1147511



Internal ID18856102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112398033..112398381hg38UCSC Ensembl
Outerchr10:114157791..114158139hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38349
hg19349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000278
SamplesKWB1
Known GenesACSL5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1147511
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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