A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641813



Internal ID6681895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11825848..11829886hg38UCSC Ensembl
Innerchr18:11825848..11829886hg38UCSC Ensembl
Outerchr18:11825348..11830386hg38UCSC Ensembl
chr18:11825847..11829885hg19UCSC Ensembl
Innerchr18:11825847..11829885hg19UCSC Ensembl
Outerchr18:11825347..11830385hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg384039
hg194039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15807379
SamplesHG01167
Known GenesGNAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641813
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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