A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641999



Internal ID7028770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:25498838..25500993hg38UCSC Ensembl
Innerchr18:25498847..25500985hg38UCSC Ensembl
Outerchr18:25498830..25501002hg38UCSC Ensembl
chr18:23078802..23080957hg19UCSC Ensembl
Innerchr18:23078811..23080949hg19UCSC Ensembl
Outerchr18:23078794..23080966hg19UCSC Ensembl
Cytoband18q11.2
Allele length
AssemblyAllele length
hg382156
hg192156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15820673, essv15820674
SamplesHG02923, HG03129
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641999
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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