A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600188



Internal ID6987232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35103991..35109622hg38UCSC Ensembl
Innerchr4:35104044..35109570hg38UCSC Ensembl
Outerchr4:35103939..35109675hg38UCSC Ensembl
chr4:35105613..35111244hg19UCSC Ensembl
Innerchr4:35105666..35111192hg19UCSC Ensembl
Outerchr4:35105561..35111297hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg385632
hg195632
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11393289, essv11393288
SamplesHG00245, NA18994
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600188
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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