A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279772



Internal ID5446086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:69077438..69078343hg38UCSC Ensembl
Innerchr15:69077488..69078293hg38UCSC Ensembl
Outerchr15:69077368..69078413hg38UCSC Ensembl
chr15:69369778..69370683hg19UCSC Ensembl
Innerchr15:69369828..69370633hg19UCSC Ensembl
Outerchr15:69369708..69370753hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38906
hg19906
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636818
Supporting Variants
SamplesNA18963
Known GenesMIR548H4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279772
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