A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638155



Internal ID7024941
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:20711755..20713745hg38UCSC Ensembl
Innerchr16:20711784..20713717hg38UCSC Ensembl
Outerchr16:20711727..20713774hg38UCSC Ensembl
chr16:20723077..20725067hg19UCSC Ensembl
Innerchr16:20723106..20725039hg19UCSC Ensembl
Outerchr16:20723049..20725096hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg381991
hg191991
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15405028, essv15405029
SamplesHG02051, HG04161
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638155
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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