A curated catalogue of human genomic structural variation




Variant Details

Variant: essv3569968



Internal ID6694664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:77290149..77290624hg38UCSC Ensembl
chr3:77339300..77339775hg19UCSC Ensembl
chr3:77421990..77422465hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38476
hg19476
hg18476
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele OriginNot tested
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv1000557
Supporting Variants
SamplesHuRef
Known GenesROBO2
MethodSequencing
Analysis
PlatformSanger Sequencing
Comments
ReferencePang_et_al_2010
Pubmed ID20482838
Accession Number(s)essv3569968
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