A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110668



Internal ID19252329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:222090114..222090179hg38UCSC Ensembl
Outerchr1:222263456..222263521hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960323
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110668
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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