A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620209



Internal ID7007081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:29179799..29188410hg38UCSC Ensembl
Innerchr9:29179799..29188410hg38UCSC Ensembl
Outerchr9:29179299..29188910hg38UCSC Ensembl
chr9:29179797..29188408hg19UCSC Ensembl
Innerchr9:29179797..29188408hg19UCSC Ensembl
Outerchr9:29179297..29188908hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg388612
hg198612
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13443117
SamplesNA18978
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620209
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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