A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601609



Internal ID6988645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102078048..102129114hg38UCSC Ensembl
Innerchr4:102078099..102129063hg38UCSC Ensembl
Outerchr4:102077997..102129165hg38UCSC Ensembl
chr4:102999205..103050271hg19UCSC Ensembl
Innerchr4:102999256..103050220hg19UCSC Ensembl
Outerchr4:102999154..103050322hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3851067
hg1951067
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11545231
SamplesHG03740
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601609
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