A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109834



Internal ID19281589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:166997226..166997279hg38UCSC Ensembl
Outerchr6:167410714..167410767hg19UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3441n106
Supporting Variantsnssv3958220
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109834
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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