A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5983863



Internal ID8961266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:10977042..10978052hg38UCSC Ensembl
chr1:11037099..11038109hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381011
hg191011
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2672799
Supporting Variants
SamplesHG00159
Known GenesC1orf127
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5983863
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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