A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1385n106



Internal ID19019494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89489792..89490492hg38UCSC Ensembl
chr16:89556200..89556900hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1144781, nsv1131121
SamplesKWS1, KWS2
Known GenesANKRD11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1385n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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