A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2896n106



Internal ID22796724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:121361094..121368945hg38UCSC Ensembl
chr4:122282249..122290100hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg387852
hg197852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1122709, nsv1129162
SamplesKWS1
Known GenesQRFPR
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2896n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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