A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3198n106



Internal ID22797026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154744623..154744946hg38UCSC Ensembl
chr5:154124183..154124506hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38324
hg19324
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1113834, nsv1131427
SamplesKWS1
Known GenesLARP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3198n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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