A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15499387



Internal ID3056754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:65107051..65111752hg38UCSC Ensembl
Innerchr16:65107051..65111752hg38UCSC Ensembl
Outerchr16:65106950..65111840hg38UCSC Ensembl
chr16:65140954..65145655hg19UCSC Ensembl
Innerchr16:65140954..65145655hg19UCSC Ensembl
Outerchr16:65140853..65145743hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg384702
hg194702
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638844
Supporting Variants
SamplesHG02687
Known GenesCDH11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15499387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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