A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998265



Internal ID19186816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:4211484..4211568hg38UCSC Ensembl
Outerchr16:4261485..4261569hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3885
hg1985
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146903
Supporting Variants
SamplesKWB1
Known GenesSRL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998265
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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