A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6558065



Internal ID9535468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:11855872..11856638hg38UCSC Ensembl
Outerchr18:11855803..11856708hg38UCSC Ensembl
Innerchr18:11855871..11856637hg19UCSC Ensembl
Outerchr18:11855802..11856707hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672629
Supporting Variants
SamplesNA19456
Known GenesGNAL
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6558065
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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