A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15319554



Internal ID3371965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91949662..91956536hg38UCSC Ensembl
Innerchr15:91949662..91956536hg38UCSC Ensembl
Outerchr15:91949478..91956746hg38UCSC Ensembl
chr15:92492892..92499766hg19UCSC Ensembl
Innerchr15:92492892..92499766hg19UCSC Ensembl
Outerchr15:92492708..92499976hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386875
hg196875
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637251
Supporting Variants
SamplesHG03021
Known GenesSLCO3A1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15319554
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