A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637696



Internal ID6677798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:4353267..4362846hg38UCSC Ensembl
Innerchr16:4353267..4362846hg38UCSC Ensembl
Outerchr16:4353058..4363084hg38UCSC Ensembl
chr16:4403268..4412847hg19UCSC Ensembl
Innerchr16:4403268..4412847hg19UCSC Ensembl
Outerchr16:4403059..4413085hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg389580
hg199580
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15363709
SamplesNA19058
Known GenesCORO7, CORO7-PAM16
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637696
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer