A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15624645



Internal ID3920188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:15365563..15368746hg38UCSC Ensembl
Innerchr17:15365563..15368746hg38UCSC Ensembl
Outerchr17:15365443..15368879hg38UCSC Ensembl
chr17:15268880..15272063hg19UCSC Ensembl
Innerchr17:15268880..15272063hg19UCSC Ensembl
Outerchr17:15268760..15272196hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg383184
hg193184
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3640069
Supporting Variants
SamplesHG03572
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15624645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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