A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6321791



Internal ID9299194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27752542..27752689hg38UCSC Ensembl
chr10:28041471..28041618hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2668102
Supporting Variants
SamplesNA18541
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6321791
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