A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620381



Internal ID7007252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:35645706..35646690hg38UCSC Ensembl
Innerchr9:35645709..35646687hg38UCSC Ensembl
Outerchr9:35645703..35646693hg38UCSC Ensembl
chr9:35645703..35646687hg19UCSC Ensembl
Innerchr9:35645706..35646684hg19UCSC Ensembl
Outerchr9:35645700..35646690hg19UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg38985
hg19985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13459408
SamplesHG03064
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620381
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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