A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638826



Internal ID7025611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63864029..63907632hg38UCSC Ensembl
Innerchr16:63864529..63907132hg38UCSC Ensembl
Outerchr16:63863029..63908632hg38UCSC Ensembl
chr16:63897933..63941536hg19UCSC Ensembl
Innerchr16:63898433..63941036hg19UCSC Ensembl
Outerchr16:63896933..63942536hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3843604
hg1943604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15498565
SamplesHG01961
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638826
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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