A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5613962



Internal ID8591365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:3635433..3637001hg38UCSC Ensembl
Outerchr18:3635396..3637051hg38UCSC Ensembl
Innerchr18:3635432..3637000hg19UCSC Ensembl
Outerchr18:3635395..3637050hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381656
hg191656
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666773
Supporting Variants
SamplesHG00702
Known GenesDLGAP1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5613962
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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