A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15344323



Internal ID4829635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99170334..99172411hg38UCSC Ensembl
Innerchr15:99170347..99172399hg38UCSC Ensembl
Outerchr15:99170322..99172424hg38UCSC Ensembl
chr15:99710539..99712616hg19UCSC Ensembl
Innerchr15:99710552..99712604hg19UCSC Ensembl
Outerchr15:99710527..99712629hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382078
hg192078
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637421
Supporting Variants
SamplesNA12046
Known GenesTTC23
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15344323
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