A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15944397



Internal ID4363916
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77102167..77103293hg38UCSC Ensembl
Innerchr18:77102217..77103243hg38UCSC Ensembl
Outerchr18:77102117..77103343hg38UCSC Ensembl
chr18:74814123..74815249hg19UCSC Ensembl
Innerchr18:74814173..74815199hg19UCSC Ensembl
Outerchr18:74814073..74815299hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg381127
hg191127
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3643203
Supporting Variants
SamplesHG03896
Known GenesMBP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15944397
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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