A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1078005



Internal ID19318121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:160613767..160633768hg38UCSC Ensembl
chr6:161034799..161054800hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3820002
hg1920002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765677
SamplesKWP1
Known GenesLPA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1078005
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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