A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1232n106



Internal ID20160589
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68420999..68421219hg38UCSC Ensembl
chr15:68713338..68713558hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38221
hg19221
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1142704, nsv1130352, nsv1129940
SamplesKWS1, KWS2
Known GenesITGA11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1232n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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