A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3096012



Internal ID10768992
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 StatusM
Merged Variants
Supporting Variantsessv7365579
SamplesHuRef
Known GenesZNF700
MethodSequencing
Analysis
PlatformComplete Genomics
Comments
ReferencePang_et_al_2013b
Pubmed ID24192839
Accession Number(s)esv3096012
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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