A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15939511



Internal ID5941327
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:76440956..76611445hg38UCSC Ensembl
chr18:74152912..74323402hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38170490
hg19170491
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643171
Supporting Variants
SamplesNA06984
Known GenesFLJ44313, LINC00908, ZNF516
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15939511
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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