A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641937



Internal ID7028708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:21393719..21395113hg38UCSC Ensembl
Innerchr18:21393722..21395111hg38UCSC Ensembl
Outerchr18:21393717..21395116hg38UCSC Ensembl
chr18:18973680..18975074hg19UCSC Ensembl
Innerchr18:18973683..18975072hg19UCSC Ensembl
Outerchr18:18973678..18975077hg19UCSC Ensembl
Cytoband18q11.1
Allele length
AssemblyAllele length
hg381395
hg191395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15818632
SamplesNA18877
Known GenesGREB1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641937
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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