A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148274



Internal ID18850548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:180639042..180639333hg38UCSC Ensembl
Outerchr5:180066042..180066333hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38292
hg19292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4001784
SamplesKWB1
Known GenesFLT4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148274
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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