A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1117e214



Internal ID22757011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98082439..98163909hg38UCSC Ensembl
chr5:97418143..97499613hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3881471
hg1981471
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3605908, esv3605907
SamplesNA20753
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1117e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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