A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622429



Internal ID6662599
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14755268..14758895hg38UCSC Ensembl
Innerchr10:14755330..14758834hg38UCSC Ensembl
Outerchr10:14755207..14758957hg38UCSC Ensembl
chr10:14797267..14800894hg19UCSC Ensembl
Innerchr10:14797329..14800833hg19UCSC Ensembl
Outerchr10:14797206..14800956hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg383628
hg193628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13704034
SamplesHG00543
Known GenesFAM107B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622429
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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