A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15264580



Internal ID4670311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:61394751..61406619hg38UCSC Ensembl
Innerchr15:61394751..61406619hg38UCSC Ensembl
Outerchr15:61394545..61406830hg38UCSC Ensembl
chr15:61686950..61698818hg19UCSC Ensembl
Innerchr15:61686950..61698818hg19UCSC Ensembl
Outerchr15:61686744..61699029hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg3811869
hg1911869
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636683
Supporting Variants
SamplesHG04195
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15264580
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