A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3643229



Internal ID7029998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:77735403..77759674hg38UCSC Ensembl
chr18:75447359..75471630hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg3824272
hg1924272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv645e214
Supporting Variantsessv15948732, essv15948733
SamplesHG02628, NA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3643229
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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