A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15524411



Internal ID6919937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75892145..75969241hg38UCSC Ensembl
Innerchr16:75892164..75969223hg38UCSC Ensembl
Outerchr16:75892127..75969260hg38UCSC Ensembl
chr16:75926043..76003139hg19UCSC Ensembl
Innerchr16:75926062..76003121hg19UCSC Ensembl
Outerchr16:75926025..76003158hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3877097
hg1977097
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639108
Supporting Variants
SamplesNA21117
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15524411
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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