A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15193295



Internal ID2632950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:26006084..26012332hg38UCSC Ensembl
Innerchr15:26006084..26012332hg38UCSC Ensembl
Outerchr15:26005584..26012832hg38UCSC Ensembl
chr15:26251231..26257479hg19UCSC Ensembl
Innerchr15:26251231..26257479hg19UCSC Ensembl
Outerchr15:26250731..26257979hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg386249
hg196249
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3635941
Supporting Variants
SamplesHG02330
Known GenesLOC100128714
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15193295
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