A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3564630



Internal ID7035730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:56351643..56359561hg38UCSC Ensembl
Outerchr19:56863012..56870930hg19UCSC Ensembl
Outerchr19:61554824..61562742hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg387919
hg197919
hg187919
Variant TypeCNV deletion
Copy Number
Allele State
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv994926
Supporting Variants
SamplesHuRef
Known Genes
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3564630
Frequency
Sample Size3
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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