A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15352170



Internal ID5353986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100508357..100603781hg38UCSC Ensembl
chr15:101048562..101143986hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg3895425
hg1995425
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637480
Supporting Variants
SamplesHG04093
Known GenesASB7, CERS3, LINS, PRKXP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15352170
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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