A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638297



Internal ID7025083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:26372168..26377129hg38UCSC Ensembl
Innerchr16:26372168..26377129hg38UCSC Ensembl
Outerchr16:26372094..26377304hg38UCSC Ensembl
chr16:26383489..26388450hg19UCSC Ensembl
Innerchr16:26383489..26388450hg19UCSC Ensembl
Outerchr16:26383415..26388625hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg384962
hg194962
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15437231, essv15437232, essv15437230
SamplesNA18599, NA18610, NA18957
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638297
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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