A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17431260



Internal ID22489130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21576661..21614395hg38UCSC Ensembl
chr7:21616279..21654013hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3837735
hg1937735
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5912460
Supporting Variants
Samples
Known GenesDNAH11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17431260
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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