A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv589n106



Internal ID19018698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:12380178..12380812hg38UCSC Ensembl
chr11:12401725..12402359hg19UCSC Ensembl
Cytoband11p15.3
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1120600, nsv1119257
SamplesKWS1
Known GenesPARVA
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv589n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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