A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767781



Internal ID18968745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161090477..161090607hg38UCSC Ensembl
chr6:161511509..161511639hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1074442
Supporting Variants
SamplesKWP1
Known GenesMAP3K4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767781
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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