A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639582



Internal ID6679673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89469830..89470949hg38UCSC Ensembl
Innerchr16:89469830..89470949hg38UCSC Ensembl
Outerchr16:89469626..89471095hg38UCSC Ensembl
chr16:89536238..89537357hg19UCSC Ensembl
Innerchr16:89536238..89537357hg19UCSC Ensembl
Outerchr16:89536034..89537503hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381120
hg191120
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15569820
SamplesHG01176
Known GenesANKRD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639582
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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