A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1146947



Internal ID19195669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:107053161..107053361hg38UCSC Ensembl
Outerchr4:107974318..107974518hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3998310
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1146947
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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