A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317318



Internal ID1895342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90509682..90516104hg38UCSC Ensembl
Innerchr15:90509682..90516104hg38UCSC Ensembl
Outerchr15:90509182..90516604hg38UCSC Ensembl
chr15:91052914..91059336hg19UCSC Ensembl
Innerchr15:91052914..91059336hg19UCSC Ensembl
Outerchr15:91052414..91059836hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg386423
hg196423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637229
Supporting Variants
SamplesHG01781
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317318
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