A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595996



Internal ID6983314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42317051..42332740hg38UCSC Ensembl
Innerchr3:42317051..42332740hg38UCSC Ensembl
Outerchr3:42316551..42333240hg38UCSC Ensembl
chr3:42358543..42374232hg19UCSC Ensembl
Innerchr3:42358543..42374232hg19UCSC Ensembl
Outerchr3:42358043..42374732hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3815690
hg1915690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10991717
SamplesNA19171
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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