A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15810197



Internal ID5812013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:11865026..11866906hg38UCSC Ensembl
Innerchr18:11865026..11866906hg38UCSC Ensembl
Outerchr18:11864773..11867305hg38UCSC Ensembl
chr18:11865025..11866905hg19UCSC Ensembl
Innerchr18:11865025..11866905hg19UCSC Ensembl
Outerchr18:11864772..11867304hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg381881
hg191881
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641818
Supporting Variants
SamplesNA19982
Known GenesGNAL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15810197
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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