A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643228



Internal ID7029997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77734972..77759107hg38UCSC Ensembl
Innerchr18:77735472..77758607hg38UCSC Ensembl
Outerchr18:77733972..77760107hg38UCSC Ensembl
chr18:75446928..75471063hg19UCSC Ensembl
Innerchr18:75447428..75470563hg19UCSC Ensembl
Outerchr18:75445928..75472063hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3824136
hg1924136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv645e214
Supporting Variantsessv15948729, essv15948730, essv15948731
SamplesHG02628, NA06984, HG03061
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643228
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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