A curated catalogue of human genomic structural variation




Variant Details

Variant: essv7365579



Internal ID10297175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:11931668..11932389hg38UCSC Ensembl
Outerchr19:12042483..12043204hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3096012
Supporting Variants
SamplesHuRef
Known GenesZNF700
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)essv7365579
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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