A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3999497



Internal ID19190089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:161090686..161090883hg38UCSC Ensembl
Outerchr6:161511718..161511915hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38198
hg19198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146290
Supporting Variants
SamplesKWB1
Known GenesMAP3K4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3999497
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer