A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15363836



Internal ID6527124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4911412..4916514hg38UCSC Ensembl
Innerchr16:4911412..4916514hg38UCSC Ensembl
Outerchr16:4910912..4917014hg38UCSC Ensembl
chr16:4961413..4966515hg19UCSC Ensembl
Innerchr16:4961413..4966515hg19UCSC Ensembl
Outerchr16:4960913..4967015hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg385103
hg195103
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637711
Supporting Variants
SamplesNA20544
Known GenesPPL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15363836
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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