A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148771



Internal ID19199296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:40794886..40794973hg38UCSC Ensembl
Outerchr3:40836377..40836464hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3997559
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148771
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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