A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620201



Internal ID7007073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:28906988..28929169hg38UCSC Ensembl
Innerchr9:28907488..28928669hg38UCSC Ensembl
Outerchr9:28905988..28930169hg38UCSC Ensembl
chr9:28906986..28929167hg19UCSC Ensembl
Innerchr9:28907486..28928667hg19UCSC Ensembl
Outerchr9:28905986..28930167hg19UCSC Ensembl
Cytoband9p21.1
Allele length
AssemblyAllele length
hg3822182
hg1922182
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13439984
SamplesHG03270
Known GenesLINGO2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620201
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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