A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641599



Internal ID6681684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:3504024..3507639hg38UCSC Ensembl
Innerchr18:3504024..3507639hg38UCSC Ensembl
Outerchr18:3503990..3507664hg38UCSC Ensembl
chr18:3504022..3507637hg19UCSC Ensembl
Innerchr18:3504022..3507637hg19UCSC Ensembl
Outerchr18:3503988..3507662hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg383616
hg193616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15779355
SamplesNA11994
Known GenesDLGAP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641599
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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