A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595857



Internal ID6983175
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv884e214
Supporting Variantsessv10980896, essv10980895
SamplesHG01384, HG01257
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595857
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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