A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665952



Internal ID9932057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52651880..52656534hg38UCSC Ensembl
Outerchr10:52651843..52656584hg38UCSC Ensembl
Innerchr10:54411640..54416294hg19UCSC Ensembl
Outerchr10:54411603..54416344hg19UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg384742
hg194742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv141e199
Supporting Variantsessv6261645
SamplesHG00345
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665952
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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