A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15362369



Internal ID2664733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1894867..1910767hg38UCSC Ensembl
Innerchr16:1894867..1910767hg38UCSC Ensembl
Outerchr16:1894367..1911267hg38UCSC Ensembl
chr16:1944868..1960768hg19UCSC Ensembl
Innerchr16:1944868..1960768hg19UCSC Ensembl
Outerchr16:1944368..1961268hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815901
hg1915901
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637625
Supporting Variants
SamplesHG02356
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15362369
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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