A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1075e214



Internal ID22756969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:16998667..17012174hg38UCSC Ensembl
chr5:16998776..17012283hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg3813508
hg1913508
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3604146, esv3604147
SamplesNA10847
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv1075e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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