A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621617



Internal ID7008485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:118084404..118089229hg38UCSC Ensembl
Innerchr9:118084433..118089201hg38UCSC Ensembl
Outerchr9:118084376..118089258hg38UCSC Ensembl
chr9:120846682..120851507hg19UCSC Ensembl
Innerchr9:120846711..120851479hg19UCSC Ensembl
Outerchr9:120846654..120851536hg19UCSC Ensembl
Cytoband9q33.1
Allele length
AssemblyAllele length
hg384826
hg194826
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13612636
SamplesHG01988
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621617
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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