A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv97n106



Internal ID20159454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:65798226..65798566hg38UCSC Ensembl
chr1:66263909..66264249hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1133861, nsv1138293
SamplesKWS1, KWS2
Known GenesPDE4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv97n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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