A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642781



Internal ID6682861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:63714650..63805844hg38UCSC Ensembl
chr18:61381884..61473078hg19UCSC Ensembl
Cytoband18q21.33
Allele length
AssemblyAllele length
hg3891195
hg1991195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15906736
SamplesNA19114
Known GenesSERPINB11, SERPINB7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642781
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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