A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6181673



Internal ID9118692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17098318..17100021hg38UCSC Ensembl
Outerchr5:17098161..17100174hg38UCSC Ensembl
Innerchr5:17098427..17100130hg19UCSC Ensembl
Outerchr5:17098270..17100283hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg382014
hg192014
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2657544
Supporting Variants
SamplesHG01133
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6181673
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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