A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5607560



Internal ID8584963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:72100674..72103369hg38UCSC Ensembl
Outerchr10:72100614..72103437hg38UCSC Ensembl
Innerchr10:73860432..73863127hg19UCSC Ensembl
Outerchr10:73860372..73863195hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg382824
hg192824
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2667465
Supporting Variants
SamplesNA19197
Known GenesASCC1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5607560
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