A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15390668



Internal ID5392484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:17241044..17275656hg38UCSC Ensembl
chr16:17334901..17369513hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg3834613
hg1934613
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638072
Supporting Variants
SamplesHG03890
Known GenesXYLT1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15390668
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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