A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602269



Internal ID6989303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:132838090..132942687hg38UCSC Ensembl
Innerchr4:132838119..132942658hg38UCSC Ensembl
Outerchr4:132838061..132942716hg38UCSC Ensembl
chr4:133759245..133863842hg19UCSC Ensembl
Innerchr4:133759274..133863813hg19UCSC Ensembl
Outerchr4:133759216..133863871hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38104598
hg19104598
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11609288
SamplesHG01989
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602269
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