A curated catalogue of human genomic structural variation




Variant Details

Variant: esv1416262



Internal ID12579384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33757389..33757464hg38UCSC Ensembl
chr19:34248294..34248369hg19UCSC Ensembl
chr19:38940134..38940209hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3876
hg1976
hg1876
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv3968585
SamplesHuRef
Known GenesCHST8
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferenceLevy_et_al_2007
Pubmed ID17803354
Accession Number(s)esv1416262
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