A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15537870



Internal ID1990605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:81718109..81720240hg38UCSC Ensembl
Innerchr16:81718128..81720222hg38UCSC Ensembl
Outerchr16:81718091..81720259hg38UCSC Ensembl
chr16:81751714..81753845hg19UCSC Ensembl
Innerchr16:81751733..81753827hg19UCSC Ensembl
Outerchr16:81751696..81753864hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg382132
hg192132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639340
Supporting Variants
SamplesHG01847
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15537870
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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