A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5770347



Internal ID9655100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:27597556..27611019hg38UCSC Ensembl
Outerchr3:27597519..27611069hg38UCSC Ensembl
Innerchr3:27639047..27652510hg19UCSC Ensembl
Outerchr3:27639010..27652560hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3813551
hg1913551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658828
Supporting Variants
SamplesNA19384
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5770347
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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