A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641773



Internal ID7028544
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:10325236..10345901hg38UCSC Ensembl
Innerchr18:10325736..10345401hg38UCSC Ensembl
Outerchr18:10324236..10346901hg38UCSC Ensembl
chr18:10325233..10345898hg19UCSC Ensembl
Innerchr18:10325733..10345398hg19UCSC Ensembl
Outerchr18:10324233..10346898hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3820666
hg1920666
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv600e214
Supporting Variantsessv15804483, essv15804482
SamplesNA21097, HG00182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641773
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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