A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3603491



Internal ID6990522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185340195..185340521hg38UCSC Ensembl
Innerchr4:185340204..185340513hg38UCSC Ensembl
Outerchr4:185340187..185340530hg38UCSC Ensembl
chr4:186261349..186261675hg19UCSC Ensembl
Innerchr4:186261358..186261667hg19UCSC Ensembl
Outerchr4:186261341..186261684hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11735933
SamplesHG00551
Known GenesSNX25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3603491
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