A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1153390



Internal ID19197197
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:234663119..234663202hg38UCSC Ensembl
Outerchr1:234798865..234798948hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001307
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1153390
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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