A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5639747



Internal ID8617150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:63130317..63501596hg38UCSC Ensembl
Outerchr10:63130283..63501631hg38UCSC Ensembl
Innerchr10:64890077..65261356hg19UCSC Ensembl
Outerchr10:64890043..65261391hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38371349
hg19371349
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677353
Supporting Variants
SamplesNA19130
Known GenesJMJD1C, JMJD1C-AS1, MIR1296, NRBF2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5639747
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