A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3602330



Internal ID6989364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:135485940..135530798hg38UCSC Ensembl
Innerchr4:135485940..135530798hg38UCSC Ensembl
Outerchr4:135485440..135531298hg38UCSC Ensembl
chr4:136407095..136451953hg19UCSC Ensembl
Innerchr4:136407095..136451953hg19UCSC Ensembl
Outerchr4:136406595..136452453hg19UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3844859
hg1944859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1027e214
Supporting Variantsessv11619923
SamplesNA20818
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3602330
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