A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151829



Internal ID19196031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:145573976..145583760hg38UCSC Ensembl
Outerchr4:146495128..146504912hg19UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg389785
hg199785
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3999011
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151829
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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