A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6126974



Internal ID9715159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119305765..119308411hg38UCSC Ensembl
chr10:121065277..121067923hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg382647
hg192647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658883
Supporting Variants
SamplesNA19468
Known GenesGRK5
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6126974
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