A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641931



Internal ID7028702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21029054..21031346hg38UCSC Ensembl
Innerchr18:21029063..21031337hg38UCSC Ensembl
Outerchr18:21029045..21031355hg38UCSC Ensembl
chr18:18609015..18611307hg19UCSC Ensembl
Innerchr18:18609024..18611298hg19UCSC Ensembl
Outerchr18:18609006..18611316hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg382293
hg192293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15818605
SamplesHG02585
Known GenesROCK1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641931
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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