A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15792894



Internal ID3289665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:5927626..5934107hg38UCSC Ensembl
Innerchr18:5927627..5934106hg38UCSC Ensembl
Outerchr18:5927625..5934108hg38UCSC Ensembl
chr18:5927625..5934106hg19UCSC Ensembl
Innerchr18:5927626..5934105hg19UCSC Ensembl
Outerchr18:5927624..5934107hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg386482
hg196482
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641661
Supporting Variants
SamplesHG02922
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15792894
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer