A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3599962



Internal ID6640224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:25410850..25412888hg38UCSC Ensembl
Innerchr4:25410870..25412868hg38UCSC Ensembl
Outerchr4:25410830..25412908hg38UCSC Ensembl
chr4:25412472..25414510hg19UCSC Ensembl
Innerchr4:25412492..25414490hg19UCSC Ensembl
Outerchr4:25412452..25414530hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg382039
hg192039
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11370936, essv11370938, essv11370937
SamplesHG02649, HG03910, NA21111
Known GenesANAPC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3599962
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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