A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639484



Internal ID7026264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:86596727..86597313hg38UCSC Ensembl
Innerchr16:86596727..86597313hg38UCSC Ensembl
Outerchr16:86596482..86597599hg38UCSC Ensembl
chr16:86630333..86630919hg19UCSC Ensembl
Innerchr16:86630333..86630919hg19UCSC Ensembl
Outerchr16:86630088..86631205hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15553844
SamplesHG00421
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639484
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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