A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6073565



Internal ID9050968
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:91962165..91962322hg38UCSC Ensembl
chr1:92427722..92427879hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg38158
hg19158
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2659029
Supporting Variants
SamplesHG00343
Known GenesBRDT
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6073565
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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