A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998367



Internal ID19193116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:17875494..17875590hg38UCSC Ensembl
Outerchr8:17733003..17733099hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3897
hg1997
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1147006
Supporting Variants
SamplesKWB1
Known GenesFGL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998367
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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