A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637698



Internal ID7024488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4580701..4598188hg38UCSC Ensembl
Innerchr16:4581201..4597688hg38UCSC Ensembl
Outerchr16:4579701..4599188hg38UCSC Ensembl
chr16:4630702..4648189hg19UCSC Ensembl
Innerchr16:4631202..4647689hg19UCSC Ensembl
Outerchr16:4629702..4649189hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3817488
hg1917488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363713, essv15363714, essv15363712
SamplesNA19917, HG03428, HG02814
Known GenesC16orf96
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637698
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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