A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622042



Internal ID6662212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:137771931..137774291hg38UCSC Ensembl
Innerchr9:137771931..137774291hg38UCSC Ensembl
Outerchr9:137771778..137774533hg38UCSC Ensembl
chr9:140666383..140668743hg19UCSC Ensembl
Innerchr9:140666383..140668743hg19UCSC Ensembl
Outerchr9:140666230..140668985hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg382361
hg192361
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13660502
SamplesHG03898
Known GenesEHMT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622042
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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