A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600333



Internal ID6987377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41418025..41447879hg38UCSC Ensembl
chr4:41420042..41449896hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3829855
hg1929855
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11405839
SamplesHG04022
Known GenesLIMCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600333
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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