A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998121



Internal ID18844574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:106535756..106536066hg38UCSC Ensembl
Outerchr6:106983631..106983941hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38311
hg19311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1153085
Supporting Variants
SamplesKWB1
Known GenesAIM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998121
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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