A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621718



Internal ID7008585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124250533..124254956hg38UCSC Ensembl
Innerchr9:124250596..124254894hg38UCSC Ensembl
Outerchr9:124250471..124255019hg38UCSC Ensembl
chr9:127012812..127017235hg19UCSC Ensembl
Innerchr9:127012875..127017173hg19UCSC Ensembl
Outerchr9:127012750..127017298hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg384424
hg194424
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618672
SamplesHG04070
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621718
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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