A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5743728



Internal ID8721131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:50422147..50430019hg38UCSC Ensembl
Outerchr10:50422113..50430054hg38UCSC Ensembl
Innerchr10:52181907..52189779hg19UCSC Ensembl
Outerchr10:52181873..52189814hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg387942
hg197942
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2670896
Supporting Variants
SamplesHG00476
Known GenesSGMS1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5743728
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