A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643200



Internal ID7029969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77007205..77027033hg38UCSC Ensembl
chr18:74719161..74738989hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3819829
hg1919829
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15943890, essv15943889, essv15943891
SamplesNA19443, NA06984, NA19316
Known GenesMBP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643200
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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