A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3604395



Internal ID6991425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24449833..24461868hg38UCSC Ensembl
Innerchr5:24449833..24461868hg38UCSC Ensembl
Outerchr5:24449333..24462368hg38UCSC Ensembl
chr5:24449942..24461977hg19UCSC Ensembl
Innerchr5:24449942..24461977hg19UCSC Ensembl
Outerchr5:24449442..24462477hg19UCSC Ensembl
Cytoband5p14.2
Allele length
AssemblyAllele length
hg3812036
hg1912036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11844071
SamplesHG02072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3604395
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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