A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600771



Internal ID6987811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64842981..64859236hg38UCSC Ensembl
chr4:65708699..65724954hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3816256
hg1916256
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11465396
SamplesHG02562
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600771
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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