A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15279667



Internal ID5281483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:68805758..68813106hg38UCSC Ensembl
Innerchr15:68805758..68813106hg38UCSC Ensembl
Outerchr15:68805709..68813384hg38UCSC Ensembl
chr15:69098097..69105445hg19UCSC Ensembl
Innerchr15:69098097..69105445hg19UCSC Ensembl
Outerchr15:69098048..69105723hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387349
hg197349
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636811
Supporting Variants
SamplesHG02888
Known GenesANP32A, ANP32A-IT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15279667
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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