A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5854977



Internal ID8832380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156761501..156762764hg38UCSC Ensembl
chr1:156731293..156732556hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg381264
hg191264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2666822
Supporting Variants
SamplesNA11893
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5854977
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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