A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv357e214



Internal ID22756251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:84054114..84128311hg38UCSC Ensembl
chr13:84628249..84702446hg19UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg3874198
hg1974198
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3632939, esv3632938
SamplesHG01354, HG00158, HG01551, HG01362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv357e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer