A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6388526



Internal ID9365929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14124096..14126911hg38UCSC Ensembl
chr10:14166095..14168910hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg382816
hg192816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663852
Supporting Variants
SamplesNA18953
Known GenesFRMD4A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6388526
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