A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639093



Internal ID6679188
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75476237..75490082hg38UCSC Ensembl
Innerchr16:75476237..75490082hg38UCSC Ensembl
Outerchr16:75475737..75490582hg38UCSC Ensembl
chr16:75510135..75523980hg19UCSC Ensembl
Innerchr16:75510135..75523980hg19UCSC Ensembl
Outerchr16:75509635..75524480hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3813846
hg1913846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15523319, essv15523320, essv15523318
SamplesNA19404, NA19917, HG03439
Known GenesCHST6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639093
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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