A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15804481



Internal ID6871569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10324631..10335502hg38UCSC Ensembl
Innerchr18:10324631..10335502hg38UCSC Ensembl
Outerchr18:10324131..10336002hg38UCSC Ensembl
chr18:10324628..10335499hg19UCSC Ensembl
Innerchr18:10324628..10335499hg19UCSC Ensembl
Outerchr18:10324128..10335999hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3810872
hg1910872
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641772
Supporting Variants
SamplesNA21097
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15804481
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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