A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15362841



Internal ID6650132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2937765..2962841hg38UCSC Ensembl
Innerchr16:2937778..2962828hg38UCSC Ensembl
Outerchr16:2937752..2962854hg38UCSC Ensembl
chr16:2987766..3012842hg19UCSC Ensembl
Innerchr16:2987779..3012829hg19UCSC Ensembl
Outerchr16:2987753..3012855hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3825077
hg1925077
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637644
Supporting Variants
SamplesNA20802
Known GenesFLYWCH1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15362841
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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