A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15496284



Internal ID493904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61579289..61585740hg38UCSC Ensembl
Innerchr16:61579289..61585740hg38UCSC Ensembl
Outerchr16:61579071..61586043hg38UCSC Ensembl
chr16:61613193..61619644hg19UCSC Ensembl
Innerchr16:61613193..61619644hg19UCSC Ensembl
Outerchr16:61612975..61619947hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg386452
hg196452
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638778
Supporting Variants
SamplesHG00174
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15496284
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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