A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15436864



Internal ID1200606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:25814357..25825583hg38UCSC Ensembl
chr16:25825678..25836904hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3811227
hg1911227
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638283
Supporting Variants
SamplesHG01072
Known GenesHS3ST4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15436864
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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