A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620407



Internal ID7007278
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13462995, essv13462996
SamplesHG03978, NA21105
Known GenesZBTB5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620407
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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