A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3619892



Internal ID7006766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:19142948..19157188hg38UCSC Ensembl
Innerchr9:19143448..19156688hg38UCSC Ensembl
Outerchr9:19141948..19158188hg38UCSC Ensembl
chr9:19142946..19157186hg19UCSC Ensembl
Innerchr9:19143446..19156686hg19UCSC Ensembl
Outerchr9:19141946..19158186hg19UCSC Ensembl
Cytoband9p22.1
Allele length
AssemblyAllele length
hg3814241
hg1914241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13415206, essv13415209, essv13415207, essv13415208
SamplesHG02582, HG02666, HG02585, NA18952
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3619892
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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