A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5945922



Internal ID8923325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:4022858..4022960hg38UCSC Ensembl
Outerchr18:4022701..4023113hg38UCSC Ensembl
Innerchr18:4022858..4022960hg19UCSC Ensembl
Outerchr18:4022701..4023113hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38413
hg19413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2675505
Supporting Variants
SamplesNA19788
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5945922
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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