A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620689



Internal ID7007559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74086800..74089745hg38UCSC Ensembl
Innerchr9:74086874..74089671hg38UCSC Ensembl
Outerchr9:74086726..74089819hg38UCSC Ensembl
chr9:76701716..76704661hg19UCSC Ensembl
Innerchr9:76701790..76704587hg19UCSC Ensembl
Outerchr9:76701642..76704735hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg382946
hg192946
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13520055, essv13520057, essv13520053, essv13520056, essv13520054, essv13520058
SamplesHG00650, NA18988, NA19068, NA18986, NA18541, NA18950
Known GenesMIR6130
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620689
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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