A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6211166



Internal ID9577473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:7836786..7842087hg38UCSC Ensembl
chr5:7836899..7842200hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg385302
hg195302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2659269
Supporting Variants
SamplesNA19147
Known GenesC5orf49
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6211166
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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