A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604435



Internal ID6991463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:25938313..25941069hg38UCSC Ensembl
Innerchr5:25938327..25941056hg38UCSC Ensembl
Outerchr5:25938300..25941083hg38UCSC Ensembl
chr5:25938422..25941178hg19UCSC Ensembl
Innerchr5:25938436..25941165hg19UCSC Ensembl
Outerchr5:25938409..25941192hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg382757
hg192757
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11845485
SamplesHG03484
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604435
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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