A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146358



Internal ID18855920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93822815..93825714hg38UCSC Ensembl
Outerchr1:94288371..94291270hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999559
SamplesKWB1
Known GenesBCAR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146358
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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