A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385624



Internal ID5387440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15465984..15470374hg38UCSC Ensembl
Innerchr16:15465984..15470374hg38UCSC Ensembl
Outerchr16:15465725..15470531hg38UCSC Ensembl
chr16:15559841..15564231hg19UCSC Ensembl
Innerchr16:15559841..15564231hg19UCSC Ensembl
Outerchr16:15559582..15564388hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg384391
hg194391
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638035
Supporting Variants
SamplesNA19440
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385624
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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