A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637266



Internal ID6677373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92584937..92600630hg38UCSC Ensembl
Innerchr15:92584937..92600630hg38UCSC Ensembl
Outerchr15:92584437..92601130hg38UCSC Ensembl
chr15:93128167..93143860hg19UCSC Ensembl
Innerchr15:93128167..93143860hg19UCSC Ensembl
Outerchr15:93127667..93144360hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg3815694
hg1915694
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv461e214
Supporting Variantsessv15320971, essv15320972
SamplesNA20911, HG01597
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637266
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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