A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385790



Internal ID5387606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15969360..15997335hg38UCSC Ensembl
chr16:16063217..16091192hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3827976
hg1927976
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638048
Supporting Variants
SamplesHG03890
Known GenesABCC1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385790
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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