A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600197



Internal ID6987241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:35625818..35628520hg38UCSC Ensembl
Innerchr4:35625835..35628504hg38UCSC Ensembl
Outerchr4:35625802..35628537hg38UCSC Ensembl
chr4:35627440..35630142hg19UCSC Ensembl
Innerchr4:35627457..35630126hg19UCSC Ensembl
Outerchr4:35627424..35630159hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg382703
hg192703
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11394155
SamplesNA20858
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600197
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