A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15374108



Internal ID5375924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:10867298..10904150hg38UCSC Ensembl
Innerchr16:10867298..10904150hg38UCSC Ensembl
Outerchr16:10866798..10904650hg38UCSC Ensembl
chr16:10961155..10998007hg19UCSC Ensembl
Innerchr16:10961155..10998007hg19UCSC Ensembl
Outerchr16:10960655..10998507hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3836853
hg1936853
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637917
Supporting Variants
SamplesHG02181
Known GenesCIITA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15374108
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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