A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2656633



Internal ID9576052
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5753983, essv5561283
SamplesHG01061, HG01073
Known GenesMANEA
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2656633
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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