A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620950



Internal ID6661131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:86081161..86082300hg38UCSC Ensembl
Innerchr9:86081162..86082299hg38UCSC Ensembl
Outerchr9:86081160..86082301hg38UCSC Ensembl
chr9:88696076..88697215hg19UCSC Ensembl
Innerchr9:88696077..88697214hg19UCSC Ensembl
Outerchr9:88696075..88697216hg19UCSC Ensembl
Cytoband9q21.33
Allele length
AssemblyAllele length
hg381140
hg191140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13544283, essv13544285, essv13544284, essv13544286
SamplesHG00100, HG01765, HG00325, HG00116
Known GenesGOLM1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620950
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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