A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999093



Internal ID19192963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:99149151..99149449hg38UCSC Ensembl
Outerchr4:100070308..100070606hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38299
hg19299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151911
Supporting Variants
SamplesKWB1
Known GenesLOC100507053
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999093
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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