A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15372238



Internal ID3428510
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9131314..9189027hg38UCSC Ensembl
Innerchr16:9131464..9188877hg38UCSC Ensembl
Outerchr16:9131164..9189177hg38UCSC Ensembl
chr16:9225171..9282884hg19UCSC Ensembl
Innerchr16:9225321..9282734hg19UCSC Ensembl
Outerchr16:9225021..9283034hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg3857714
hg1957714
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637865
Supporting Variants
SamplesHG03063
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15372238
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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