A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112144



Internal ID18908407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:159934669..159934817hg38UCSC Ensembl
Outerchr6:160355701..160355849hg19UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg38149
hg19149
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3426n106
Supporting Variantsnssv3965835
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112144
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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