A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15726578



Internal ID5500366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:67272439..67316984hg38UCSC Ensembl
chr17:65268555..65313100hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3844546
hg1944546
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641078
Supporting Variants
SamplesNA18985
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15726578
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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