A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643123



Internal ID7029892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:74623637..74695240hg38UCSC Ensembl
chr18:72335593..72407196hg19UCSC Ensembl
Cytoband18q22.3
Allele length
AssemblyAllele length
hg3871604
hg1971604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15934119
SamplesNA06984
Known GenesZNF407
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643123
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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