A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639368



Internal ID6679462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:82654364..82659642hg38UCSC Ensembl
Innerchr16:82654373..82659634hg38UCSC Ensembl
Outerchr16:82654356..82659651hg38UCSC Ensembl
chr16:82687969..82693247hg19UCSC Ensembl
Innerchr16:82687978..82693239hg19UCSC Ensembl
Outerchr16:82687961..82693256hg19UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg385279
hg195279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15542556
SamplesHG02628
Known GenesCDH13
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639368
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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