A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615734



Internal ID7002622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158599831..158624097hg38UCSC Ensembl
chr7:158392523..158416789hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3824267
hg1924267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1348e214
Supporting Variantsessv13053041, essv13053042
SamplesHG02420, HG01182
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615734
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer