A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599624



Internal ID6639888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:10476161..10518729hg38UCSC Ensembl
chr4:10477785..10520353hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3842569
hg1942569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11355318
SamplesNA18510
Known GenesCLNK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599624
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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