A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3028n106



Internal ID22796856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:3499139..3499477hg38UCSC Ensembl
chr5:3499253..3499591hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1135631, nsv1131276, nsv1111664
SamplesKWS2, KWS1
Known GenesLINC01019, LOC102467075
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3028n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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