A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11073905



Internal ID1075721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:96340862..96351459hg38UCSC Ensembl
Innerchr3:96340890..96351432hg38UCSC Ensembl
Outerchr3:96340835..96351487hg38UCSC Ensembl
chr3:96059706..96070303hg19UCSC Ensembl
Innerchr3:96059734..96070276hg19UCSC Ensembl
Outerchr3:96059679..96070331hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg3810598
hg1910598
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3597068
Supporting Variants
SamplesNA20506
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11073905
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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