A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148412



Internal ID19197818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:150181268..150181508hg38UCSC Ensembl
Outerchr3:149899055..149899295hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg38241
hg19241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000450
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148412
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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