A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5912037



Internal ID22687252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80958960..80991968hg38UCSC Ensembl
chr7:80588276..80621284hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3833009
hg1933009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17439827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5912037
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