A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6359711



Internal ID9337114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:31054694..31055180hg38UCSC Ensembl
Outerchr13:31054637..31055239hg38UCSC Ensembl
Innerchr13:31628831..31629317hg19UCSC Ensembl
Outerchr13:31628774..31629376hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38603
hg19603
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2678978
Supporting Variants
SamplesNA18499
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6359711
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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