A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641772



Internal ID7028543
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15804481, essv15804480
SamplesNA21097, HG00142
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641772
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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