A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1029e199



Internal ID22758802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96367445..96370742hg38UCSC Ensembl
chr5:95703149..95706446hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg383298
hg193298
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678579, esv2669983
SamplesNA19466, NA19443, NA19313, NA19372, HG01048, NA19445, NA19462, NA19347, NA19455, NA19461, NA19449, NA19434, HG01551, NA19331, NA19324, NA19467, NA19360, NA19468, NA19312, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1029e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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