A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3995908



Internal ID19188557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:180860162..180860292hg38UCSC Ensembl
Outerchr3:180577950..180578080hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146751
Supporting Variants
SamplesKWB1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3995908
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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