A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641600



Internal ID6681685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3523616..3524777hg38UCSC Ensembl
Innerchr18:3523616..3524777hg38UCSC Ensembl
Outerchr18:3523483..3524940hg38UCSC Ensembl
chr18:3523614..3524775hg19UCSC Ensembl
Innerchr18:3523614..3524775hg19UCSC Ensembl
Outerchr18:3523481..3524938hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg381162
hg191162
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15779356
SamplesNA18621
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641600
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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