A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13462996



Internal ID6889379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:37445402..37452136hg38UCSC Ensembl
Innerchr9:37445423..37452115hg38UCSC Ensembl
Outerchr9:37445381..37452157hg38UCSC Ensembl
chr9:37445399..37452133hg19UCSC Ensembl
Innerchr9:37445420..37452112hg19UCSC Ensembl
Outerchr9:37445378..37452154hg19UCSC Ensembl
Cytoband9p13.2
Allele length
AssemblyAllele length
hg386735
hg196735
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3620407
Supporting Variants
SamplesNA21105
Known GenesZBTB5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13462996
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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