A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601044



Internal ID6641302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76077088..76078563hg38UCSC Ensembl
Innerchr4:76077117..76078534hg38UCSC Ensembl
Outerchr4:76077059..76078592hg38UCSC Ensembl
chr4:76998241..76999716hg19UCSC Ensembl
Innerchr4:76998270..76999687hg19UCSC Ensembl
Outerchr4:76998212..76999745hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg381476
hg191476
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11507606
SamplesNA19726
Known GenesART3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601044
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