A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607689



Internal ID6994621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177411541..177415733hg38UCSC Ensembl
Innerchr5:177411561..177415714hg38UCSC Ensembl
Outerchr5:177411522..177415753hg38UCSC Ensembl
chr5:176838542..176842734hg19UCSC Ensembl
Innerchr5:176838562..176842715hg19UCSC Ensembl
Outerchr5:176838523..176842754hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384193
hg194193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12143379
SamplesNA20798
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607689
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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