A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11061855



Internal ID2450103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:85338323..85357223hg38UCSC Ensembl
chr3:85387473..85406373hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3818901
hg1918901
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596834
Supporting Variants
SamplesHG02154
Known GenesCADM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11061855
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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