A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638035



Internal ID6678133
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15385624, essv15385625, essv15385626, essv15385623, essv15385622
SamplesNA20342, NA19461, NA19428, NA19440, HG03240
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638035
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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