A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13432865



Internal ID3614259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:25496442..25525075hg38UCSC Ensembl
Innerchr9:25496446..25525071hg38UCSC Ensembl
Outerchr9:25496438..25525079hg38UCSC Ensembl
chr9:25496440..25525073hg19UCSC Ensembl
Innerchr9:25496444..25525069hg19UCSC Ensembl
Outerchr9:25496436..25525077hg19UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3828634
hg1928634
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620080
Supporting Variants
SamplesHG03202
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13432865
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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