A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603832



Internal ID6990863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:2302854..2308417hg38UCSC Ensembl
Innerchr5:2303354..2307917hg38UCSC Ensembl
Outerchr5:2301854..2309417hg38UCSC Ensembl
chr5:2302968..2308531hg19UCSC Ensembl
Innerchr5:2303468..2308031hg19UCSC Ensembl
Outerchr5:2301968..2309531hg19UCSC Ensembl
Cytoband5p15.33
Allele length
AssemblyAllele length
hg385564
hg195564
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11788538, essv11788539
SamplesHG03995, HG03896
Known GenesLOC100506858
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603832
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer