A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7064n223



Internal ID22810032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111371071..111709416hg38UCSC Ensembl
chr7:111011127..111349472hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38338346
hg19338346
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv6606166, nsv6616144, nsv6601268, nsv6602374
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)dgv7064n223
Frequency
Sample Size19652
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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