A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5753983



Internal ID8731386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:95581884..95582303hg38UCSC Ensembl
Outerchr6:95581727..95582456hg38UCSC Ensembl
Innerchr6:96029760..96030179hg19UCSC Ensembl
Outerchr6:96029603..96030332hg19UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656633
Supporting Variants
SamplesHG01061
Known GenesMANEA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5753983
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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