A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130532



Internal ID19258849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:13882318..13883621hg38UCSC Ensembl
Outerchr6:13882549..13883852hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg381304
hg191304
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3274n106
Supporting Variantsnssv3966840
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130532
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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