A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363797



Internal ID6749103
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4719936..4722366hg38UCSC Ensembl
Innerchr16:4719936..4722366hg38UCSC Ensembl
Outerchr16:4719561..4722701hg38UCSC Ensembl
chr16:4769937..4772367hg19UCSC Ensembl
Innerchr16:4769937..4772367hg19UCSC Ensembl
Outerchr16:4769562..4772702hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382431
hg192431
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637701
Supporting Variants
SamplesNA20864
Known GenesANKS3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363797
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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