A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13538729



Internal ID6912527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:81795169..81805355hg38UCSC Ensembl
Innerchr9:81795193..81805332hg38UCSC Ensembl
Outerchr9:81795146..81805379hg38UCSC Ensembl
chr9:84410084..84420270hg19UCSC Ensembl
Innerchr9:84410108..84420247hg19UCSC Ensembl
Outerchr9:84410061..84420294hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg3810187
hg1910187
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620873
Supporting Variants
SamplesNA21114
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13538729
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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