A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074366



Internal ID19322620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4020777..4020828hg38UCSC Ensembl
chr6:4021011..4021062hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771314
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074366
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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