A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5597165



Internal ID8574568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:10546892..10547113hg38UCSC Ensembl
Outerchr18:10546855..10547163hg38UCSC Ensembl
Innerchr18:10546889..10547110hg19UCSC Ensembl
Outerchr18:10546852..10547160hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg38309
hg19309
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667923
Supporting Variants
SamplesNA19720
Known GenesNAPG
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5597165
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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