A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3578396



Internal ID6703092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132191518..132191846hg38UCSC Ensembl
chr10:134005022..134005350hg19UCSC Ensembl
chr10:133855012..133855340hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38329
hg19329
hg18329
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1008205
Supporting Variants
SamplesHuRef
Known GenesDPYSL4
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3578396
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