A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605913



Internal ID6992850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98302415..98307904hg38UCSC Ensembl
Innerchr5:98302415..98307904hg38UCSC Ensembl
Outerchr5:98302177..98308167hg38UCSC Ensembl
chr5:97638119..97643608hg19UCSC Ensembl
Innerchr5:97638119..97643608hg19UCSC Ensembl
Outerchr5:97637881..97643871hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg385490
hg195490
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11989767
SamplesHG02271
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605913
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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