A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5890285



Internal ID9052023
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:36276043..36276832hg38UCSC Ensembl
Outerchr18:36276006..36276882hg38UCSC Ensembl
Innerchr18:33856006..33856795hg19UCSC Ensembl
Outerchr18:33855969..33856845hg19UCSC Ensembl
Cytoband18q12.2
Allele length
AssemblyAllele length
hg38877
hg19877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2664992
Supporting Variants
SamplesHG00699
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5890285
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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