A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121661



Internal ID18918108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166162706..166162805hg38UCSC Ensembl
Outerchr6:166576194..166576293hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968308
SamplesKWS2
Known GenesT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121661
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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