A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14848217



Internal ID5922631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:90883943..90926847hg38UCSC Ensembl
chr13:91536197..91579101hg19UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3842905
hg1942905
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633139
Supporting Variants
SamplesNA19332
Known GenesLINC00410
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14848217
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