A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603129



Internal ID6990161
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:169857119..169871027hg38UCSC Ensembl
Innerchr4:169857619..169870527hg38UCSC Ensembl
Outerchr4:169856119..169872027hg38UCSC Ensembl
chr4:170778270..170792178hg19UCSC Ensembl
Innerchr4:170778770..170791678hg19UCSC Ensembl
Outerchr4:170777270..170793178hg19UCSC Ensembl
Cytoband4q33
Allele length
AssemblyAllele length
hg3813909
hg1913909
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11690422
SamplesNA21137
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603129
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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