A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13587904



Internal ID1593820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:102731067..102777914hg38UCSC Ensembl
Innerchr9:102731067..102777914hg38UCSC Ensembl
Outerchr9:102730567..102778414hg38UCSC Ensembl
chr9:105493349..105540196hg19UCSC Ensembl
Innerchr9:105493349..105540196hg19UCSC Ensembl
Outerchr9:105492849..105540696hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg3846848
hg1946848
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3621290
Supporting Variants
SamplesHG01485
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13587904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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