A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637935



Internal ID6678034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:11726890..11731232hg38UCSC Ensembl
Innerchr16:11726925..11731197hg38UCSC Ensembl
Outerchr16:11726855..11731267hg38UCSC Ensembl
chr16:11820746..11825088hg19UCSC Ensembl
Innerchr16:11820781..11825053hg19UCSC Ensembl
Outerchr16:11820711..11825123hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg384343
hg194343
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377012
SamplesHG04186
Known GenesTXNDC11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637935
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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