A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496278



Internal ID1460637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61289449..61374938hg38UCSC Ensembl
Innerchr16:61289949..61374438hg38UCSC Ensembl
Outerchr16:61288449..61375938hg38UCSC Ensembl
chr16:61323353..61408842hg19UCSC Ensembl
Innerchr16:61323853..61408342hg19UCSC Ensembl
Outerchr16:61322353..61409842hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3885490
hg1985490
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638772
Supporting Variants
SamplesHG01351
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496278
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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