A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1154121



Internal ID19196101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:140286445..140288946hg38UCSC Ensembl
Outerchr4:141207599..141210100hg19UCSC Ensembl
Cytoband4q31.1
Allele length
AssemblyAllele length
hg382502
hg192502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003402
SamplesKWB1
Known GenesLOC100129858, SCOC
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1154121
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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