A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596834



Internal ID6984148
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11061856, essv11061854, essv11061855
SamplesNA20346, HG02154, HG02095
Known GenesCADM2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596834
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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