A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10898297



Internal ID900113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1037506..1232159hg38UCSC Ensembl
chr3:1079190..1273843hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38194654
hg19194654
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3594942
Supporting Variants
SamplesHG00264
Known GenesCNTN6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10898297
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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