A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372779



Internal ID6777186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9584087..9667901hg38UCSC Ensembl
Innerchr16:9584087..9667901hg38UCSC Ensembl
Outerchr16:9583587..9668401hg38UCSC Ensembl
chr16:9677944..9761758hg19UCSC Ensembl
Innerchr16:9677944..9761758hg19UCSC Ensembl
Outerchr16:9677444..9762258hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3883815
hg1983815
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637874
Supporting Variants
SamplesNA20878
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372779
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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