A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10980896



Internal ID1507307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:36354858..36376120hg38UCSC Ensembl
chr3:36396350..36417612hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3821263
hg1921263
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595857
Supporting Variants
SamplesHG01384
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10980896
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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