A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1315n106



Internal ID22795143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20767219..20767600hg38UCSC Ensembl
chr16:20778541..20778922hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg38382
hg19382
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121160, nsv1111519, nsv1126177
SamplesKWS2, KWS1
Known GenesACSM3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1315n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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