A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1100051



Internal ID11916489
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:20624372..20624539hg38UCSC Ensembl
chr19:20807178..20807345hg19UCSC Ensembl
chr19:20599018..20599185hg18UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38168
hg19168
hg18168
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv4282100
SamplesHuRef
Known GenesZNF626
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1100051
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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