A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607680



Internal ID6994612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:177011103..177012567hg38UCSC Ensembl
Innerchr5:177011103..177012567hg38UCSC Ensembl
Outerchr5:177010776..177012916hg38UCSC Ensembl
chr5:176438104..176439568hg19UCSC Ensembl
Innerchr5:176438104..176439568hg19UCSC Ensembl
Outerchr5:176437777..176439917hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381465
hg191465
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12142447
SamplesHG00524
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607680
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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