A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6281882



Internal ID9625169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:62064578..62065762hg38UCSC Ensembl
chr10:63824337..63825521hg19UCSC Ensembl
Cytoband10q21.2
Allele length
AssemblyAllele length
hg381185
hg191185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2677112
Supporting Variants
SamplesNA19338
Known GenesARID5B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6281882
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