A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1073606



Internal ID18971803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:161350667..161351068hg38UCSC Ensembl
chr6:161771699..161772100hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38402
hg19402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3761999
SamplesKWP1
Known GenesPARK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1073606
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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