A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15248855



Internal ID5619741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51988719..52016225hg38UCSC Ensembl
Innerchr15:51989219..52015725hg38UCSC Ensembl
Outerchr15:51987719..52017225hg38UCSC Ensembl
chr15:52280916..52308422hg19UCSC Ensembl
Innerchr15:52281416..52307922hg19UCSC Ensembl
Outerchr15:52279916..52309422hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3827507
hg1927507
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636476
Supporting Variants
SamplesNA19043
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15248855
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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