A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620744



Internal ID7007614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:76534909..76545848hg38UCSC Ensembl
Innerchr9:76534927..76545830hg38UCSC Ensembl
Outerchr9:76534891..76545866hg38UCSC Ensembl
chr9:79149825..79160764hg19UCSC Ensembl
Innerchr9:79149843..79160746hg19UCSC Ensembl
Outerchr9:79149807..79160782hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3810940
hg1910940
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13528406, essv13528402, essv13528404, essv13528401, essv13528403, essv13528405
SamplesHG01675, HG00239, HG02219, HG00125, HG00123, NA19770
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620744
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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