A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385618



Internal ID5387434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15432577..15440058hg38UCSC Ensembl
chr16:15526434..15533915hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg387482
hg197482
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638033
Supporting Variants
SamplesNA19434
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385618
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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