A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3617938



Internal ID6658133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:88025337..88043428hg38UCSC Ensembl
chr8:89037565..89055656hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3818092
hg1918092
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13251531, essv13251530
SamplesHG01177, HG01162
Known GenesMMP16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3617938
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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