A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13648196



Internal ID3378833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:134994145..134994721hg38UCSC Ensembl
Innerchr9:134994151..134994715hg38UCSC Ensembl
Outerchr9:134994139..134994727hg38UCSC Ensembl
chr9:137885991..137886567hg19UCSC Ensembl
Innerchr9:137885997..137886561hg19UCSC Ensembl
Outerchr9:137885985..137886573hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621972
Supporting Variants
SamplesHG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13648196
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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