A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3605916



Internal ID6992853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:98480399..98499401hg38UCSC Ensembl
Innerchr5:98480399..98499401hg38UCSC Ensembl
Outerchr5:98479899..98499901hg38UCSC Ensembl
chr5:97816103..97835105hg19UCSC Ensembl
Innerchr5:97816103..97835105hg19UCSC Ensembl
Outerchr5:97815603..97835605hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg3819003
hg1919003
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11989782
SamplesHG01607
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3605916
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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