A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3620890



Internal ID7007760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:82747310..82748677hg38UCSC Ensembl
Innerchr9:82747314..82748674hg38UCSC Ensembl
Outerchr9:82747307..82748681hg38UCSC Ensembl
chr9:85362225..85363592hg19UCSC Ensembl
Innerchr9:85362229..85363589hg19UCSC Ensembl
Outerchr9:85362222..85363596hg19UCSC Ensembl
Cytoband9q21.32
Allele length
AssemblyAllele length
hg381368
hg191368
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13538828
SamplesHG01974
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3620890
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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