A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15317352



Internal ID5300493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:90652514..90661815hg38UCSC Ensembl
Innerchr15:90652526..90661804hg38UCSC Ensembl
Outerchr15:90652503..90661827hg38UCSC Ensembl
chr15:91195745..91205046hg19UCSC Ensembl
Innerchr15:91195757..91205035hg19UCSC Ensembl
Outerchr15:91195734..91205058hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg389302
hg199302
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637231
Supporting Variants
SamplesNA18757
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15317352
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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