A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621228



Internal ID7008097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:100171650..100183448hg38UCSC Ensembl
Innerchr9:100171650..100183448hg38UCSC Ensembl
Outerchr9:100171150..100183948hg38UCSC Ensembl
chr9:102933932..102945730hg19UCSC Ensembl
Innerchr9:102933932..102945730hg19UCSC Ensembl
Outerchr9:102933432..102946230hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3811799
hg1911799
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13580289, essv13580290
SamplesNA19794, HG01479
Known GenesINVS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621228
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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