A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619772



Internal ID7006646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:15218973..15221675hg38UCSC Ensembl
Innerchr9:15219023..15221625hg38UCSC Ensembl
Outerchr9:15218887..15221761hg38UCSC Ensembl
chr9:15218971..15221673hg19UCSC Ensembl
Innerchr9:15219021..15221623hg19UCSC Ensembl
Outerchr9:15218885..15221759hg19UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13408025, essv13408026
SamplesHG03091, HG02139
Known GenesTTC39B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619772
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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