A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15293106



Internal ID4092032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75599912..75609522hg38UCSC Ensembl
Innerchr15:75600412..75609022hg38UCSC Ensembl
Outerchr15:75598912..75610522hg38UCSC Ensembl
chr15:75892253..75901863hg19UCSC Ensembl
Innerchr15:75892753..75901363hg19UCSC Ensembl
Outerchr15:75891253..75902863hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg389611
hg199611
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636927
Supporting Variants
SamplesHG03717
Known GenesSNUPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15293106
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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