A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1074909



Internal ID19317551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:11044166..11044467hg38UCSC Ensembl
chr6:11044399..11044700hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765958
SamplesKWP1
Known GenesELOVL2, ELOVL2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1074909
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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