A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15481288



Internal ID2157766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:55267400..55268145hg38UCSC Ensembl
Innerchr16:55267424..55268121hg38UCSC Ensembl
Outerchr16:55267376..55268169hg38UCSC Ensembl
chr16:55301312..55302057hg19UCSC Ensembl
Innerchr16:55301336..55302033hg19UCSC Ensembl
Outerchr16:55301288..55302081hg19UCSC Ensembl
Cytoband16q12.2
Allele length
AssemblyAllele length
hg38746
hg19746
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638682
Supporting Variants
SamplesHG01951
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15481288
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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