A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998682



Internal ID18846044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91140671..91140972hg38UCSC Ensembl
Outerchr8:92152899..92153200hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1149896
Supporting Variants
SamplesKWB1
Known GenesLRRC69
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998682
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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