A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636219



Internal ID7023015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39780197..39791512hg38UCSC Ensembl
Innerchr15:39780697..39791012hg38UCSC Ensembl
Outerchr15:39779197..39792512hg38UCSC Ensembl
chr15:40072398..40083713hg19UCSC Ensembl
Innerchr15:40072898..40083213hg19UCSC Ensembl
Outerchr15:40071398..40084713hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3811316
hg1911316
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15227690
SamplesHG00445
Known GenesFSIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636219
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