A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12905068



Internal ID6657665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98520750..98533961hg38UCSC Ensembl
chr7:98150062..98163273hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3813212
hg1913212
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614258
Supporting Variants
SamplesNA20805
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12905068
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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