A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638245



Internal ID7025031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24250312..24252016hg38UCSC Ensembl
Innerchr16:24250326..24252002hg38UCSC Ensembl
Outerchr16:24250298..24252030hg38UCSC Ensembl
chr16:24261633..24263337hg19UCSC Ensembl
Innerchr16:24261647..24263323hg19UCSC Ensembl
Outerchr16:24261619..24263351hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381705
hg191705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15429974
SamplesHG03085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638245
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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