A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9744477



Internal ID18372037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1625942..1626005hg38UCSC Ensembl
chr10:1668137..1668200hg19UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3545730
Supporting Variants
Samples
Known GenesADARB2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9744477
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer