A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614870



Internal ID7001763
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124379728..124390251hg38UCSC Ensembl
Innerchr7:124379759..124390221hg38UCSC Ensembl
Outerchr7:124379698..124390282hg38UCSC Ensembl
chr7:124019782..124030305hg19UCSC Ensembl
Innerchr7:124019813..124030275hg19UCSC Ensembl
Outerchr7:124019752..124030336hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3810524
hg1910524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12949299
SamplesHG02888
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614870
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