A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642616



Internal ID6682696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:56653495..56670399hg38UCSC Ensembl
chr18:54320726..54337630hg19UCSC Ensembl
Cytoband18q21.31
Allele length
AssemblyAllele length
hg3816905
hg1916905
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15888726, essv15888727
SamplesHG02888, HG02610
Known GenesWDR7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642616
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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