A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14701061



Internal ID477713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39360099..39361415hg38UCSC Ensembl
Innerchr13:39360149..39361292hg38UCSC Ensembl
Outerchr13:39359769..39361745hg38UCSC Ensembl
chr13:39934236..39935552hg19UCSC Ensembl
Innerchr13:39934286..39935429hg19UCSC Ensembl
Outerchr13:39933906..39935882hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg381317
hg191317
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3631831
Supporting Variants
SamplesHG00157
Known GenesLHFP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14701061
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