A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074899



Internal ID19324394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:133199..202100hg38UCSC Ensembl
chr6:133199..202100hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3868902
hg1968902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3767925
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074899
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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